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Low-set ears

DA: 53

Developmental anomaly information

Definition: Low-set ears refer to abnormalities in the position of the outer ear (pinna or auricle).

Synonyms:

Misplaced ear

Developmental anomaly parent: (empty)	Topology: Human body > Head and neck > Head > Face > Ears
System: Human body > Nervous system > Sensory organs > Ears	Developmental anomaly category: Malformation

Case records MDB9, MDB17, MDB21, MDB22, MDB29, MDB47, MDB48, MDB66, MDB68, MDB69, MDB70, MDB72, MDB96, MDB101, MDB103, MDB109, MDB112, MDB124, MDB134, MDB136, MDB339, MDB151, MDB166, MDB181, MDB186, MDB175, MDB196, MDB198, MDB201, MDB60, MDB205, MDB209, MDB211, MDB214, MDB215, MDB216, MDB217, MDB223, MDB225, MDB226, MDB227, MDB238, MDB242, MDB249, MDB258, MDB260, MDB261, MDB287, MDB298, MDB312, MDB310, MDB319, MDB321, MDB325, MDB327, MDB331, MDB332, MDB343, MDB350, MDB352, MDB359, MDB362, MDB380, MDB387, MDB390, MDB399, MDB402, MDB404, MDB410, MDB419, MDB53, MDB424, MDB427, MDB428, MDB437, MDB441, MDB443, MDB459, MDB470, MDB471, MDB473, MDB476, MDB483, MDB485, MDB489, MDB491, MDB503, MDB504, MDB506, MDB515, MDB518, MDB520, MDB522, MDB527, MDB44, MDB543, MDB34, MDB106, MDB140, MDB146, MDB150, MDB162, MDB168, MDB171, MDB257, MDB270, MDB292, MDB329, MDB326, MDB100, MDB268

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Humpath: 28

Observed in MDB cases

Observed in combinaisons (MDB)

Observed in malformative diseases (MDB)

() in cases MDB, MDB, MDB, MDB, MDB

Associated genes in profile

Associated genes in malformative diseases

Associated chromosomal diseases

Associated signaling pathways

Associated developmental anomalies

Here is the list of developmental anomalies associated with this developmental anomaly, based on the cases' information :

Facial dysmorphism 5.9% (70/1187 anomalies), in cases MDB9, MDB17, MDB21, MDB29, MDB47, MDB48, MDB68, MDB70, MDB72, MDB96, MDB101, MDB109, MDB112, MDB124, MDB134, MDB136, MDB339, MDB151, MDB166, MDB186, MDB198, MDB205, MDB214, MDB215, MDB216, MDB217, MDB226, MDB227, MDB238, MDB258, MDB260, MDB261, MDB312, MDB319, MDB321, MDB327, MDB331, MDB332, MDB350, MDB352, MDB359, MDB390, MDB399, MDB402, MDB410, MDB53, MDB424, MDB427, MDB437, MDB443, MDB459, MDB470, MDB471, MDB473, MDB504, MDB506, MDB515, MDB518, MDB520, MDB522, MDB44, MDB543, MDB34, MDB106, MDB168, MDB171, MDB257, MDB270, MDB329, MDB100
Placenta hypoplasia 3.37% (40/1187 anomalies), in cases MDB22, MDB29, MDB47, MDB48, MDB101, MDB103, MDB136, MDB339, MDB196, MDB201, MDB209, MDB215, MDB223, MDB242, MDB249, MDB258, MDB261, MDB287, MDB310, MDB321, MDB332, MDB359, MDB387, MDB419, MDB471, MDB473, MDB483, MDB491, MDB503, MDB504, MDB520, MDB522, MDB543, MDB140, MDB162, MDB171, MDB329, MDB326, MDB100, MDB268
Pulmonary hypoplasia 3.12% (37/1187 anomalies), in cases MDB9, MDB22, MDB29, MDB69, MDB103, MDB109, MDB181, MDB186, MDB175, MDB201, MDB209, MDB211, MDB214, MDB223, MDB225, MDB226, MDB227, MDB238, MDB261, MDB325, MDB327, MDB359, MDB380, MDB404, MDB443, MDB471, MDB483, MDB503, MDB518, MDB44, MDB150, MDB168, MDB171, MDB329, MDB326, MDB100, MDB268
Intrauterine growth retardation, symmetric 2.86% (34/1187 anomalies), in cases MDB22, MDB72, MDB101, MDB103, MDB136, MDB339, MDB215, MDB223, MDB225, MDB249, MDB310, MDB321, MDB332, MDB343, MDB343, MDB359, MDB380, MDB387, MDB390, MDB399, MDB404, MDB53, MDB471, MDB473, MDB476, MDB483, MDB489, MDB520, MDB522, MDB140, MDB162, MDB168, MDB270, MDB329
Hypertelorism 2.53% (30/1187 anomalies), in cases MDB47, MDB69, MDB72, MDB96, MDB124, MDB136, MDB151, MDB166, MDB181, MDB196, MDB198, MDB214, MDB215, MDB217, MDB227, MDB238, MDB321, MDB331, MDB352, MDB459, MDB473, MDB485, MDB491, MDB515, MDB520, MDB522, MDB527, MDB257, MDB270, MDB100
Low nasal bridge 1.77% (21/1187 anomalies), in cases MDB9, MDB66, MDB69, MDB103, MDB181, MDB223, MDB260, MDB287, MDB298, MDB331, MDB350, MDB387, MDB410, MDB443, MDB470, MDB471, MDB515, MDB44, MDB146, MDB292, MDB268
Micrognathia 1.77% (21/1187 anomalies), in cases MDB9, MDB17, MDB48, MDB101, MDB134, MDB196, MDB60, MDB209, MDB216, MDB217, MDB238, MDB242, MDB287, MDB312, MDB310, MDB380, MDB404, MDB473, MDB489, MDB171, MDB257
Retrognathia 1.77% (21/1187 anomalies), in cases MDB21, MDB136, MDB339, MDB332, MDB350, MDB359, MDB399, MDB402, MDB437, MDB470, MDB471, MDB476, MDB503, MDB504, MDB506, MDB518, MDB543, MDB146, MDB168, MDB270, MDB100
Talipes equinovarus, bilateral 1.52% (18/1187 anomalies), in cases MDB29, MDB103, MDB112, MDB181, MDB205, MDB209, MDB215, MDB223, MDB238, MDB310, MDB327, MDB331, MDB362, MDB428, MDB140, MDB150, MDB257, MDB292
Short neck 1.52% (18/1187 anomalies), in cases MDB175, MDB215, MDB225, MDB260, MDB298, MDB319, MDB331, MDB343, MDB387, MDB428, MDB441, MDB470, MDB476, MDB506, MDB140, MDB270, MDB329, MDB268
Neck edema 1.43% (17/1187 anomalies), in cases MDB17, MDB29, MDB69, MDB109, MDB198, MDB227, MDB310, MDB321, MDB404, MDB419, MDB443, MDB470, MDB476, MDB506, MDB520, MDB543, MDB292
Broad nasal bridge 1.26% (15/1187 anomalies), in cases MDB47, MDB48, MDB124, MDB181, MDB196, MDB198, MDB215, MDB226, MDB321, MDB427, MDB504, MDB520, MDB527, MDB326, MDB100
Clindodactyly of 5th finger, bilateral 1.26% (15/1187 anomalies), in cases MDB48, MDB69, MDB96, MDB196, MDB215, MDB217, MDB226, MDB319, MDB331, MDB350, MDB362, MDB387, MDB515, MDB140, MDB168
Microretrognathia 1.26% (15/1187 anomalies), in cases MDB103, MDB109, MDB181, MDB201, MDB223, MDB258, MDB325, MDB327, MDB331, MDB410, MDB424, MDB427, MDB520, MDB292, MDB326
Triangular face 1.18% (14/1187 anomalies), in cases MDB22, MDB186, MDB201, MDB223, MDB327, MDB332, MDB359, MDB390, MDB399, MDB53, MDB437, MDB522, MDB34, MDB106
Prominent and pointed nose 1.18% (14/1187 anomalies), in cases MDB201, MDB201, MDB216, MDB217, MDB242, MDB327, MDB332, MDB352, MDB390, MDB428, MDB437, MDB470, MDB34, MDB106
Microcephaly 1.01% (12/1187 anomalies), in cases MDB17, MDB21, MDB22, MDB68, MDB166, MDB175, MDB60, MDB258, MDB473, MDB150, MDB329, MDB326
Macroglossia 0.93% (11/1187 anomalies), in cases MDB17, MDB72, MDB186, MDB175, MDB211, MDB227, MDB319, MDB343, MDB527, MDB171, MDB270
Adrenal hypoplasia, fetal 0.93% (11/1187 anomalies), in cases MDB72, MDB186, MDB175, MDB196, MDB201, MDB211, MDB380, MDB404, MDB459, MDB520, MDB168
Nonimmune hydrops fetalis (NIHF) 0.84% (10/1187 anomalies), in cases MDB72, MDB109, MDB339, MDB214, MDB225, MDB483, MDB485, MDB162, MDB168, MDB257
Single transverse palmar crease, unilateral 0.84% (10/1187 anomalies), in cases MDB136, MDB242, MDB260, MDB319, MDB321, MDB331, MDB387, MDB410, MDB270, MDB268
Single umblical artery (SUA)-Isolated 0.76% (9/1187 anomalies), in cases MDB9, MDB70, MDB209, MDB215, MDB325, MDB359, MDB53, MDB427, MDB428
Overlapping fingers 0.76% (9/1187 anomalies), in cases MDB22, MDB101, MDB175, MDB201, MDB238, MDB399, MDB489, MDB518, MDB100
Clindodactyly of 5th finger, unilateral 0.76% (9/1187 anomalies), in cases MDB22, MDB136, MDB166, MDB216, MDB287, MDB53, MDB518, MDB522, MDB146
Lobulated, fused and horseshoe kidney 0.76% (9/1187 anomalies), in cases MDB48, MDB101, MDB310, MDB332, MDB359, MDB380, MDB399, MDB53, MDB257
Flattened nose 0.76% (9/1187 anomalies), in cases MDB66, MDB209, MDB214, MDB223, MDB258, MDB325, MDB140, MDB329, MDB100
Coarctation of aorta, 0.76% (9/1187 anomalies), in cases MDB96, MDB101, MDB136, MDB225, MDB402, MDB53, MDB427, MDB489, MDB268
Ventricular septal defect, membranous 0.76% (9/1187 anomalies), in cases MDB109, MDB205, MDB310, MDB331, MDB387, MDB404, MDB470, MDB506, MDB326
Toe hypoplasia, first, bilateral 0.76% (9/1187 anomalies), in cases MDB242, MDB310, MDB350, MDB362, MDB402, MDB441, MDB489, MDB146, MDB150
Omphalocele 0.67% (8/1187 anomalies), in cases MDB9, MDB22, MDB70, MDB109, MDB249, MDB325, MDB359, MDB100
Ventricular septal defect, muscular 0.67% (8/1187 anomalies), in cases MDB22, MDB101, MDB390, MDB399, MDB53, MDB515, MDB257, MDB329
Long philtrum 0.67% (8/1187 anomalies), in cases MDB29, MDB68, MDB518, MDB44, MDB150, MDB257, MDB270, MDB329
Macrocephaly 0.67% (8/1187 anomalies), in cases MDB47, MDB66, MDB69, MDB70, MDB60, MDB217, MDB437, MDB100
Hypogenesis of the Cerebellar Vermis 0.67% (8/1187 anomalies), in cases MDB69, MDB60, MDB310, MDB352, MDB359, MDB427, MDB443, MDB329
Sloping forehead 0.67% (8/1187 anomalies), in cases MDB69, MDB112, MDB198, MDB201, MDB226, MDB258, MDB327, MDB326
Retroplacental hemorrhage 0.67% (8/1187 anomalies), in cases MDB70, MDB134, MDB186, MDB485, MDB543, MDB34, MDB150, MDB326
Potter deformity sequence 0.67% (8/1187 anomalies), in cases MDB103, MDB181, MDB209, MDB223, MDB325, MDB485, MDB503, MDB150
Transverse palmar crease, bilateral 0.67% (8/1187 anomalies), in cases MDB124, MDB134, MDB227, MDB362, MDB441, MDB443, MDB515, MDB146
Large anterior fontanelle 0.67% (8/1187 anomalies), in cases MDB60, MDB53, MDB428, MDB470, MDB471, MDB476, MDB543, MDB106
Flat face 0.59% (7/1187 anomalies), in cases MDB68, MDB186, MDB227, MDB298, MDB485, MDB44, MDB150
Wide space between 1st and 2nd toes, bilateral 0.59% (7/1187 anomalies), in cases MDB96, MDB196, MDB216, MDB287, MDB437, MDB470, MDB150
Badly-hemmed ears 0.59% (7/1187 anomalies), in cases MDB166, MDB186, MDB175, MDB60, MDB205, MDB214, MDB326
Arthrogryposis 0.59% (7/1187 anomalies), in cases MDB238, MDB485, MDB520, MDB522, MDB543, MDB257, MDB329
Epicanthus 0.51% (6/1187 anomalies), in cases MDB29, MDB124, MDB134, MDB151, MDB214, MDB217
Narrow thorax 0.51% (6/1187 anomalies), in cases MDB66, MDB196, MDB223, MDB471, MDB518, MDB44
Frontal bossing 0.51% (6/1187 anomalies), in cases MDB68, MDB70, MDB196, MDB223, MDB471, MDB257
Hexadactyly, postaxial 0.51% (6/1187 anomalies), in cases MDB68, MDB109, MDB181, MDB321, MDB168, MDB326
Corpus callosum agenesis 0.51% (6/1187 anomalies), in cases MDB166, MDB258, MDB441, MDB443, MDB473, MDB329
Exophthalmos, bilateral 0.42% (5/1187 anomalies), in cases MDB47, MDB175, MDB343, MDB527, MDB140
Nephromegaly, bilateral 0.42% (5/1187 anomalies), in cases MDB68, MDB109, MDB181, MDB459, MDB146
Mongoloid slope of the palpebral fissures 0.42% (5/1187 anomalies), in cases MDB68, MDB227, MDB410, MDB419, MDB515
Rocker-bottom feet 0.42% (5/1187 anomalies), in cases MDB68, MDB196, MDB205, MDB515, MDB522
Cleft palate with cleft lip (CLP), median 0.42% (5/1187 anomalies), in cases MDB109, MDB112, MDB166, MDB60, MDB504
Right bilobate lung 0.42% (5/1187 anomalies), in cases MDB109, MDB196, MDB215, MDB226, MDB518
Intestinal malrotation 0.42% (5/1187 anomalies), in cases MDB136, MDB399, MDB402, MDB504, MDB100
Large nose, fetal 0.42% (5/1187 anomalies), in cases MDB175, MDB312, MDB527, MDB543, MDB171
Potter's facies 0.42% (5/1187 anomalies), in cases MDB209, MDB223, MDB485, MDB146, MDB150
Cystic hygroma 0.42% (5/1187 anomalies), in cases MDB225, MDB260, MDB168, MDB257, MDB329
Cleft palate, bilateral 0.42% (5/1187 anomalies), in cases MDB238, MDB249, MDB332, MDB168, MDB257
Aberrant right subclavian artery 0.34% (4/1187 anomalies), in cases MDB22, MDB209, MDB404, MDB268
Giant omphalocele 0.34% (4/1187 anomalies), in cases MDB29, MDB53, MDB473, MDB491
Multicystic renal dysplasia,bilateral 0.34% (4/1187 anomalies), in cases MDB29, MDB181, MDB215, MDB150
Hydrocephalus 0.34% (4/1187 anomalies), in cases MDB47, MDB60, MDB217, MDB100
Polysplenia 0.34% (4/1187 anomalies), in cases MDB68, MDB181, MDB150, MDB326
Cerebral ventriculomegaly 0.34% (4/1187 anomalies), in cases MDB69, MDB60, MDB217, MDB520
Syndactyly, simple (webbed), fingers 0.34% (4/1187 anomalies), in cases MDB69, MDB72, MDB238, MDB53
Right atrium Enlargement 0.34% (4/1187 anomalies), in cases MDB109, MDB136, MDB201, MDB326
Thymic hypoplasia 0.34% (4/1187 anomalies), in cases MDB109, MDB483, MDB518, MDB326
Semilobar holoprosencephaly 0.34% (4/1187 anomalies), in cases MDB166, MDB60, MDB258, MDB473
Cerebellar hypoplasia 0.34% (4/1187 anomalies), in cases MDB181, MDB60, MDB310, MDB329
Bladder hypoplasia 0.34% (4/1187 anomalies), in cases MDB181, MDB209, MDB310, MDB503
Anencephaly facies 0.34% (4/1187 anomalies), in cases MDB175, MDB211, MDB527, MDB140
Short philtrum 0.34% (4/1187 anomalies), in cases MDB196, MDB198, MDB258, MDB473
Polydactyly of the hand, preaxial 0.34% (4/1187 anomalies), in cases MDB60, MDB249, MDB380, MDB473
Tetralogy of Fallot 0.34% (4/1187 anomalies), in cases MDB205, MDB491, MDB504, MDB326
Pulmonary artery hypoplasia 0.34% (4/1187 anomalies), in cases MDB205, MDB380, MDB504, MDB326
Imperforate Anus 0.34% (4/1187 anomalies), in cases MDB209, MDB325, MDB402, MDB150
Cleft palate with cleft lip,bilateral, complete 0.34% (4/1187 anomalies), in cases MDB261, MDB402, MDB459, MDB326
Brachydactyly 0.34% (4/1187 anomalies), in cases MDB287, MDB362, MDB441, MDB483
Triploidy, Maternal, nonmolar (triploidy by digyny) 0.34% (4/1187 anomalies), in cases MDB332, MDB380, MDB543, MDB171
Limbs hypoplasia 0.34% (4/1187 anomalies), in cases MDB471, MDB483, MDB44, MDB106
Ascites, fetal 0.25% (3/1187 anomalies), in cases MDB9, MDB109, MDB214
Communicating hydrocephalus 0.25% (3/1187 anomalies), in cases MDB17, MDB21, MDB443
Tracheoesophageal fistula (TEF), and esophageal atresia, Type C 0.25% (3/1187 anomalies), in cases MDB22, MDB22, MDB257
Foot edema 0.25% (3/1187 anomalies), in cases MDB29, MDB520, MDB162
Hypotelorisme 0.25% (3/1187 anomalies), in cases MDB68, MDB504, MDB326
Thalamic nuclei centrum medianum fusion 0.25% (3/1187 anomalies), in cases MDB68, MDB258, MDB329
Dandy-Walker malformation 0.25% (3/1187 anomalies), in cases MDB69, MDB352, MDB427
Fingers amputation 0.25% (3/1187 anomalies), in cases MDB69, MDB112, MDB166
Meckel diverticulum 0.25% (3/1187 anomalies), in cases MDB101, MDB136, MDB326
Syndactyly of the feet , simple (webbed), unilateral 0.25% (3/1187 anomalies), in cases MDB101, MDB196, MDB310
Right ventricle dilatation 0.25% (3/1187 anomalies), in cases MDB109, MDB136, MDB201
Polydactyly of both fingers & toes, postaxial 0.25% (3/1187 anomalies), in cases MDB136, MDB427, MDB459
Relative Macrocephaly 0.25% (3/1187 anomalies), in cases MDB151, MDB196, MDB518
Olfactory bulbs, absence of 0.25% (3/1187 anomalies), in cases MDB166, MDB181, MDB258
Polymicrogyria, focal 0.25% (3/1187 anomalies), in cases MDB181, MDB329, MDB329
Deep gray nuclear malformations(the caudate nuclei, thalami,..) 0.25% (3/1187 anomalies), in cases MDB181, MDB60, MDB473
Micropenis 0.25% (3/1187 anomalies), in cases MDB196, MDB402, MDB326
Renal hypoplasia 0.25% (3/1187 anomalies), in cases MDB196, MDB287, MDB171
Atrioventricular - channel 0.25% (3/1187 anomalies), in cases MDB201, MDB260, MDB410
Renal agenesis, bilateral 0.25% (3/1187 anomalies), in cases MDB209, MDB402, MDB518
Cleft palate, median posterior 0.25% (3/1187 anomalies), in cases MDB215, MDB518, MDB527
Microphthalmia 0.25% (3/1187 anomalies), in cases MDB215, MDB261, MDB257
Absence of one paire the rib 0.25% (3/1187 anomalies), in cases MDB227, MDB483, MDB326
Decreased skull bone mineralization 0.25% (3/1187 anomalies), in cases MDB261, MDB106, MDB292
Long umbilical cord 0.25% (3/1187 anomalies), in cases MDB310, MDB522, MDB150
Renal pelvis dilatation, unilateral 0.25% (3/1187 anomalies), in cases MDB321, MDB53, MDB146
Renal agenesis, unilateral 0.25% (3/1187 anomalies), in cases MDB325, MDB503, MDB150
Syndactyly of the fingers, complex, bilateral 0.25% (3/1187 anomalies), in cases MDB332, MDB402, MDB171
Anencephaly 0.25% (3/1187 anomalies), in cases MDB343, MDB527, MDB140
Scoliosis, congenital 0.17% (2/1187 anomalies), in cases MDB9, MDB238
Dolicocephaly 0.17% (2/1187 anomalies), in cases MDB21, MDB134
Persistent left superior vena cava 0.17% (2/1187 anomalies), in cases MDB22, MDB209
vertebral bones and gracile ribs with multiple abnormalities 0.17% (2/1187 anomalies), in cases MDB29, MDB150
Lumbosacral agenesis 0.17% (2/1187 anomalies), in cases MDB47, MDB518
Thin upper lip 0.17% (2/1187 anomalies), in cases MDB47, MDB44
Pes cavus 0.17% (2/1187 anomalies), in cases MDB48, MDB72
Lymphedema of the neck 0.17% (2/1187 anomalies), in cases MDB66, MDB70
Flattened occiput 0.17% (2/1187 anomalies), in cases MDB68, MDB227
Nasal hypoplasia 0.17% (2/1187 anomalies), in cases MDB69, MDB483
Constriction Ring Deformity of the upper limbs 0.17% (2/1187 anomalies), in cases MDB69, MDB166
Syndactyly of the toes, complex, bilateral 0.17% (2/1187 anomalies), in cases MDB69, MDB332
Pterygium colli 0.17% (2/1187 anomalies), in cases MDB69, MDB321
Gracile ribs 0.17% (2/1187 anomalies), in cases MDB69, MDB109
Bowing of femur, congenital 0.17% (2/1187 anomalies), in cases MDB69, MDB223
Aortic valve atresia 0.17% (2/1187 anomalies), in cases MDB101, MDB332
Placenta circumvallata 0.17% (2/1187 anomalies), in cases MDB103, MDB485
Patent Foramen Ovale 0.17% (2/1187 anomalies), in cases MDB109, MDB201
Tricuspid valve dysplasia 0.17% (2/1187 anomalies), in cases MDB109, MDB473
Wide space between 1st and 2nd toes, unilateral 0.17% (2/1187 anomalies), in cases MDB124, MDB327
Pulmonary artery dilatation, fetal 0.17% (2/1187 anomalies), in cases MDB136, MDB332
Aortic valve stenosis, congenital 0.17% (2/1187 anomalies), in cases MDB136, MDB201
Defective developement of left ventricle 0.17% (2/1187 anomalies), in cases MDB136, MDB201
Dysplasia of deep nuclei (olive dysplasia) 0.17% (2/1187 anomalies), in cases MDB151, MDB257
Gastroschisis 0.17% (2/1187 anomalies), in cases MDB166, MDB518
Renal-hepatic-pancreatic dysplasia 0.17% (2/1187 anomalies), in cases MDB181, MDB146
Glial heterotopia, multi-focal 0.17% (2/1187 anomalies), in cases MDB181, MDB258
Meroanencephaly 0.17% (2/1187 anomalies), in cases MDB186, MDB211
Rachischisis, cervical 0.17% (2/1187 anomalies), in cases MDB175, MDB343
Ureteral duplication, complete, unilateral 0.17% (2/1187 anomalies), in cases MDB175, MDB146
Bulbous nose 0.17% (2/1187 anomalies), in cases MDB196, MDB443
Intrauterine growth retardation, asymmetric 0.17% (2/1187 anomalies), in cases MDB196, MDB312
Renal pelvis dilatation, bilateral 0.17% (2/1187 anomalies), in cases MDB198, MDB489
Camptodactyly, bilateral 0.17% (2/1187 anomalies), in cases MDB201, MDB504
Hypoplasia of ascending aorta 0.17% (2/1187 anomalies), in cases MDB201, MDB205
Microtia 0.17% (2/1187 anomalies), in cases MDB60, MDB410
Flexion contracture of upper limbs 0.17% (2/1187 anomalies), in cases MDB60, MDB503
Dysplastic kidney with tubular cysts 0.17% (2/1187 anomalies), in cases MDB60, MDB503
Pulmonary valve atresia 0.17% (2/1187 anomalies), in cases MDB205, MDB504
Right ventricular hypertrophy 0.17% (2/1187 anomalies), in cases MDB205, MDB504
Arhinia 0.17% (2/1187 anomalies), in cases MDB205, MDB261
Ureter agenesis, bilateral 0.17% (2/1187 anomalies), in cases MDB209, MDB402
Diaphragmatic hernia, congenital 0.17% (2/1187 anomalies), in cases MDB211, MDB100
Unilobate lung, unilateral 0.17% (2/1187 anomalies), in cases MDB215, MDB518
Axillary pterygia, bilateral 0.17% (2/1187 anomalies), in cases MDB238, MDB150
Syndactyly of the fingers, complex, unilateral 0.17% (2/1187 anomalies), in cases MDB249, MDB380
Hypogenesis of pyramidal tracts 0.17% (2/1187 anomalies), in cases MDB258, MDB257
Single cerebral ventricule 0.17% (2/1187 anomalies), in cases MDB258, MDB473
Brachycephaly 0.17% (2/1187 anomalies), in cases MDB331, MDB268
Stenosis of aqueduct of Sylvius 0.17% (2/1187 anomalies), in cases MDB352, MDB257
Hydrocephalus, Non-communicating 0.17% (2/1187 anomalies), in cases MDB352, MDB257
Syndactyly of the toes, unilateral 0.17% (2/1187 anomalies), in cases MDB380, MDB171
Renal focal cystic dilatation of collecting tubules 0.17% (2/1187 anomalies), in cases MDB380, MDB100
hypoplasia of the rib 0.17% (2/1187 anomalies), in cases MDB53, MDB473
Aplasia cutis congenita, scalp 0.17% (2/1187 anomalies), in cases MDB427, MDB504
Absence of the Septum Pellucidum 0.17% (2/1187 anomalies), in cases MDB441, MDB443
Interauricular communication 0.17% (2/1187 anomalies), in cases MDB473, MDB326
Small mouth 0.17% (2/1187 anomalies), in cases MDB483, MDB257
Hypoplasia of the liver 0.17% (2/1187 anomalies), in cases MDB483, MDB168
Short umbilical cord 0.17% (2/1187 anomalies), in cases MDB483, MDB491
Hydronephrosis, congenital, bilateral 0.17% (2/1187 anomalies), in cases MDB489, MDB329
Hypoplasia of diaphragm 0.17% (2/1187 anomalies), in cases MDB491, MDB506
Ureter agenesis, unilateral 0.17% (2/1187 anomalies), in cases MDB503, MDB150
Dextroposition of aorta 0.17% (2/1187 anomalies), in cases MDB504, MDB326
Bowing of long bones 0.17% (2/1187 anomalies), in cases MDB106, MDB292
Osteogenesis imperfecta, Type II 0.17% (2/1187 anomalies), in cases MDB106, MDB292
Hand edema 0.17% (2/1187 anomalies), in cases MDB150, MDB162
Varus deviation of fingers 0.08% (1/1187 anomalies), in case MDB9
Absence of innominate (brachiocephalic) vein 0.08% (1/1187 anomalies), in case MDB22
Axillary pterygia,unilateral 0.08% (1/1187 anomalies), in case MDB29
Tridactyly, unilateral 0.08% (1/1187 anomalies), in case MDB29
Tetra-amelia 0.08% (1/1187 anomalies), in case MDB47
Thanatophoric dysplasia (Type I) 0.08% (1/1187 anomalies), in case MDB66
Platyspondyly 0.08% (1/1187 anomalies), in case MDB66
Holoprosencephaly, alobar 0.08% (1/1187 anomalies), in case MDB68
Microstomia 0.08% (1/1187 anomalies), in case MDB68
Vertex aplasia cutis (ACC) 0.08% (1/1187 anomalies), in case MDB68
Cebocephaly 0.08% (1/1187 anomalies), in case MDB68
Cleft lip, unilateral 0.08% (1/1187 anomalies), in case MDB69
Holoprosencephaly 0.08% (1/1187 anomalies), in case MDB69
Constriction Ring Deformity of the lower limbs 0.08% (1/1187 anomalies), in case MDB69
Ring constriction deformity of the toes 0.08% (1/1187 anomalies), in case MDB69
Toes amputation 0.08% (1/1187 anomalies), in case MDB69
Nasal asymetria 0.08% (1/1187 anomalies), in case MDB69
Incomplete and partial hydatidiform mole 0.08% (1/1187 anomalies), in case MDB72
Diandric triploidy 0.08% (1/1187 anomalies), in case MDB72
Cleft lip 0.08% (1/1187 anomalies), in case MDB72
Left ventricular hypotrophy 0.08% (1/1187 anomalies), in case MDB96
Syndactyly of the feet , simple (webbed), bilateral 0.08% (1/1187 anomalies), in case MDB101
Turned-up nose 0.08% (1/1187 anomalies), in case MDB101
Bone mineralization defect 0.08% (1/1187 anomalies), in case MDB103
Splenomegaly, congenital 0.08% (1/1187 anomalies), in case MDB109
Polydactyly of the foot 0.08% (1/1187 anomalies), in case MDB112
Infarcted placenta 0.08% (1/1187 anomalies), in case MDB134
Periventricular Leukomalacia (PVL) 0.08% (1/1187 anomalies), in case MDB134
Renal hypoplasia, bilateral 0.08% (1/1187 anomalies), in case MDB339
Exencephaly 0.08% (1/1187 anomalies), in case MDB166
Optic nerve, absence of, bilateral 0.08% (1/1187 anomalies), in case MDB166
Cortical dysgenesis (CD), diffuse 0.08% (1/1187 anomalies), in case MDB166
Absence of hippocampal commissure 0.08% (1/1187 anomalies), in case MDB166
Encephalocele, occipital 0.08% (1/1187 anomalies), in case MDB181
Periventricular heterotopia (PH) 0.08% (1/1187 anomalies), in case MDB181
Ureter hypoplasia 0.08% (1/1187 anomalies), in case MDB181
putamen nuclei absence 0.08% (1/1187 anomalies), in case MDB181
Corticospinal tract absence 0.08% (1/1187 anomalies), in case MDB181
Placental amniotic bands 0.08% (1/1187 anomalies), in case MDB186
Marginal subchorionic hematoma 0.08% (1/1187 anomalies), in case MDB186
Holoanencephaly 0.08% (1/1187 anomalies), in case MDB175
Arachnodactyly of the toes 0.08% (1/1187 anomalies), in case MDB196
5th toe hypoplasia 0.08% (1/1187 anomalies), in case MDB196
Hand clenching, fetal 0.08% (1/1187 anomalies), in case MDB196
Flexion contracture of the fingers 0.08% (1/1187 anomalies), in case MDB196
Arachnodactyly 0.08% (1/1187 anomalies), in case MDB196
Short and dorsiflexed great toe 0.08% (1/1187 anomalies), in case MDB196
Abnormally aligned ribs 0.08% (1/1187 anomalies), in case MDB196
Small round skull 0.08% (1/1187 anomalies), in case MDB201
Double Outlet Right Ventricle, Without Transposition and VSD 0.08% (1/1187 anomalies), in case MDB201
Transverse aortic hypoplasia 0.08% (1/1187 anomalies), in case MDB201
Cerebral cyst 0.08% (1/1187 anomalies), in case MDB201
Preauricular hamartoma 0.08% (1/1187 anomalies), in case MDB60
Cryptophthalmos 0.08% (1/1187 anomalies), in case MDB60
absence of nasal septum 0.08% (1/1187 anomalies), in case MDB60
Hypoplasia of eye 0.08% (1/1187 anomalies), in case MDB60
skin hamartoma 0.08% (1/1187 anomalies), in case MDB60
Aqueduct of Sylvius atresia 0.08% (1/1187 anomalies), in case MDB60
Cerebral commissures agenesis 0.08% (1/1187 anomalies), in case MDB60
Cleft palate with cleft lip, unilateral, complete 0.08% (1/1187 anomalies), in case MDB205
wrist hyperextension, unilateral 0.08% (1/1187 anomalies), in case MDB205
Cubital deviation of the hand, unilateral 0.08% (1/1187 anomalies), in case MDB205
Prostate hypoplasia 0.08% (1/1187 anomalies), in case MDB209
Pericardial effusion 0.08% (1/1187 anomalies), in case MDB209
Googly eyes 0.08% (1/1187 anomalies), in case MDB211
Esophageal duplication,tubular form 0.08% (1/1187 anomalies), in case MDB211
Encephalocele, parietal 0.08% (1/1187 anomalies), in case MDB211
Pleural effusion, fetal 0.08% (1/1187 anomalies), in case MDB214
Micromelia 0.08% (1/1187 anomalies), in case MDB215
Prominence of nasofrontal angle 0.08% (1/1187 anomalies), in case MDB217
Placental cysts 0.08% (1/1187 anomalies), in case MDB223
Renal hypertropy, fetal, bilateral 0.08% (1/1187 anomalies), in case MDB238
Arthrogryposis,lower limbs 0.08% (1/1187 anomalies), in case MDB249
Neuronal migration anomaly 0.08% (1/1187 anomalies), in case MDB258
Olfactory nerve, absence of, bilateral 0.08% (1/1187 anomalies), in case MDB258
Micro Multicystic kidneys, medullary type 0.08% (1/1187 anomalies), in case MDB260
Acrocephaly 0.08% (1/1187 anomalies), in case MDB261
Wide space between 4th and 5th toes, unilateral 0.08% (1/1187 anomalies), in case MDB312
Foot valgus 0.08% (1/1187 anomalies), in case MDB312
short nose 0.08% (1/1187 anomalies), in case MDB319
Levocardia 0.08% (1/1187 anomalies), in case MDB319
Flexion contracture of lower limbs 0.08% (1/1187 anomalies), in case MDB325
Popliteal pterygium 0.08% (1/1187 anomalies), in case MDB325
Scoliosis, thoracic, left 0.08% (1/1187 anomalies), in case MDB325
Multicystic renal dysplasia, unilateral 0.08% (1/1187 anomalies), in case MDB325
Micromelia, lower limbs 0.08% (1/1187 anomalies), in case MDB325
flexion contracture of the forearm 0.08% (1/1187 anomalies), in case MDB325
Rib fusions 0.08% (1/1187 anomalies), in case MDB325
Large ear, fetal 0.08% (1/1187 anomalies), in case MDB325
Dorsiflexion of foot, unilateral 0.08% (1/1187 anomalies), in case MDB325
Scalloping of the frontal bones 0.08% (1/1187 anomalies), in case MDB325
Cubital pterygium, bilateral 0.08% (1/1187 anomalies), in case MDB325
Talipes equinovarus,unilateral 0.08% (1/1187 anomalies), in case MDB325
Overlapping toes 0.08% (1/1187 anomalies), in case MDB327
Placental hypermaturity 0.08% (1/1187 anomalies), in case MDB332
Narrow palate 0.08% (1/1187 anomalies), in case MDB343
Tonsillar herniation of the cerebellum 0.08% (1/1187 anomalies), in case MDB352
Malformed ear 0.08% (1/1187 anomalies), in case MDB359
Toe hypoplasia, unilateral 0.08% (1/1187 anomalies), in case MDB380
Fraser syndrome 0.08% (1/1187 anomalies), in case MDB402
Subglottic Stenosis (CSS) 0.08% (1/1187 anomalies), in case MDB402
Non-segmented lung 0.08% (1/1187 anomalies), in case MDB402
Bladder agenesis 0.08% (1/1187 anomalies), in case MDB402
Left side appendix 0.08% (1/1187 anomalies), in case MDB402
Pyloric stenosis 0.08% (1/1187 anomalies), in case MDB402
Amnion nodosum 0.08% (1/1187 anomalies), in case MDB402
left carotid artery, aberrant 0.08% (1/1187 anomalies), in case MDB404
Radial ray agenesis, unilateral 0.08% (1/1187 anomalies), in case MDB53
Cystic dilatation of the fourth ventricle 0.08% (1/1187 anomalies), in case MDB427
Anomalous pulmonary veins connection to superior & inferior vena cava 0.08% (1/1187 anomalies), in case MDB427
Hypoplastic left atrium and ventricle 0.08% (1/1187 anomalies), in case MDB427
Hypoplastic right atrium 0.08% (1/1187 anomalies), in case MDB427
Brachydactyly of the toes 0.08% (1/1187 anomalies), in case MDB428
Hepatomegaly, fetal 0.08% (1/1187 anomalies), in case MDB428
Dextrocardia, isolated 0.08% (1/1187 anomalies), in case MDB437
Nasal Clefts 0.08% (1/1187 anomalies), in case MDB437
Hypospadias, penile 0.08% (1/1187 anomalies), in case MDB459
Micromulticystic kidneys 0.08% (1/1187 anomalies), in case MDB459
Incomplete cleavage of cerebral hemispheres 0.08% (1/1187 anomalies), in case MDB473
Myelomeningocele,thoracolumbar 0.08% (1/1187 anomalies), in case MDB473
Polydactyly,of the hand, postaxial 0.08% (1/1187 anomalies), in case MDB473
Pulmonary valve dysplasia 0.08% (1/1187 anomalies), in case MDB473
Encephalocele, frontal 0.08% (1/1187 anomalies), in case MDB483
Asplenia 0.08% (1/1187 anomalies), in case MDB483
Absence of diaphragm, left 0.08% (1/1187 anomalies), in case MDB483
Hypoplasia of the pancreas 0.08% (1/1187 anomalies), in case MDB483
rudimentary heart, congenital 0.08% (1/1187 anomalies), in case MDB483
Clavicle, absence of 0.08% (1/1187 anomalies), in case MDB483
small intestinal atresia and stenosis 0.08% (1/1187 anomalies), in case MDB483
Vascular insufficiency of peripheral limb,lower limbs 0.08% (1/1187 anomalies), in case MDB485
Ureterovesical junction stenosis 0.08% (1/1187 anomalies), in case MDB489
Renal ectopia,crossed 0.08% (1/1187 anomalies), in case MDB503
Bicornuate uterus 0.08% (1/1187 anomalies), in case MDB503
Cutaneous bud 0.08% (1/1187 anomalies), in case MDB504
Agenesia of internal genital organs 0.08% (1/1187 anomalies), in case MDB518
Persistent truncus arteriosus 0.08% (1/1187 anomalies), in case MDB518
Right aortic arch 0.08% (1/1187 anomalies), in case MDB518
Rachischisis 0.08% (1/1187 anomalies), in case MDB518
Vertebral hypoplasia, dorsolumbar 0.08% (1/1187 anomalies), in case MDB518
Rib deformation with abnormal numbers, bilateral 0.08% (1/1187 anomalies), in case MDB518
Underdeveloped pelvic bones 0.08% (1/1187 anomalies), in case MDB518
Partial agenesis of the corpus callosum (PACC) 0.08% (1/1187 anomalies), in case MDB520
Hypoplasia of the humerus, bilateral 0.08% (1/1187 anomalies), in case MDB522
Chondrodysplasia punctata 0.08% (1/1187 anomalies), in case MDB44
Macrostomia 0.08% (1/1187 anomalies), in case MDB543
Bones and gracile ribs with multiple fractures 0.08% (1/1187 anomalies), in case MDB106
Thumb agenesis, unilateral 0.08% (1/1187 anomalies), in case MDB140
Radial deviation of the hand, unilateral 0.08% (1/1187 anomalies), in case MDB140
Autosomal Recessive Polycystic Kidney Disease 0.08% (1/1187 anomalies), in case MDB146
Ambiguous genitalia 0.08% (1/1187 anomalies), in case MDB150
Persistent cloaca 0.08% (1/1187 anomalies), in case MDB150
Malpositioned thumb, bilateral 0.08% (1/1187 anomalies), in case MDB150
Unilobate lung, bilateral 0.08% (1/1187 anomalies), in case MDB257
Holoprosencephaly, lobar 0.08% (1/1187 anomalies), in case MDB329
Megacystis 0.08% (1/1187 anomalies), in case MDB329
Dilatation of ureter , bilateral, congenital 0.08% (1/1187 anomalies), in case MDB329
Prominent upper lip 0.08% (1/1187 anomalies), in case MDB329
Hydromyelia 0.08% (1/1187 anomalies), in case MDB329
Micromelia, lower limb, unilateral 0.08% (1/1187 anomalies), in case MDB329

Terminology and coding

	WHO ICD-10: Q17.4

References

No reference related to Low-set ears is available at the moment.

Last modified: 2008-12-04 16:59:13 by farideh

Created: 2008-02-25 01:00:00 by phsaw

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