Joubert syndrome locus 6 JBTS6

DIS: 35




Joubert syndrome locus 6 JBTS6

Definition: (empty)


Synonyms:
There are no synonyms for this malformative disease.

Category: Monogenic disease

Developmental anomalies

Listed in the disease's profile :


There are no developmental anomalies for this disease.

Observed in MDB cases: (graph view)


There are no developmental anomalies for this disease.
Case records

Associated signaling pathways
Associations
Array
(
    [MalformativeDisease] => Array
        (
            [id] => 35
            [name] => Joubert syndrome locus 6 JBTS6
            [description] => 
            [category_id] => 2
            [gene_id] => 
            [chromosomal_anomaly_id] => 
            [infectious_agent_id] => 
            [toxic_agent_id] => 
            [maternal_condition_id] => 
            [omim_ref] => 
            [humpath_ref] => 
            [snomed_ref] => 
            [adicap_ref] => 
            [orphanet_ref] => 
            [emedicine_ref] => 
            [fetusnet_ref] => 
            [possum_ref] => 
            [ICD10_ref] => 
            [diseasesdb_ref] => 
            [mesh_ref] => 
            [wiki_ref] => 
        )

    [Category] => Array
        (
            [id] => 2
            [name] => Monogenic disease
            [description] => 
        )

    [InfectiousAgent] => Array
        (
            [id] => 
            [name] => 
            [description] => 
        )

    [ToxicAgent] => Array
        (
            [id] => 
            [name] => 
            [description] => 
        )

    [MaternalCondition] => Array
        (
            [id] => 
            [name] => 
            [description] => 
        )

    [Gene] => Array
        (
            [id] => 
            [code] => 
            [HUGO_code] => 
            [protein_name] => 
            [chromosomal_region_id] => 
            [function_id] => 
            [omim_ref] => 
            [humpath_ref] => 
            [gentests_ref] => 
            [entrez_ref] => 
            [uniprot_ref] => 
            [ensembl_ref] => 
            [orphanet_ref] => 
            [mint_ref] => 
            [gencard_ref] => 
        )

    [ChromosomalAnomaly] => Array
        (
            [id] => 
            [abbreviation] => 
            [name] => 
            [chromosome_id] => 
            [from_region] => 
            [to_region] => 
            [anomaly_id] => 
            [category_id] => 
            [humpath_ref] => 
        )

    [Diagnosis] => Array
        (
        )

    [DiseaseSynonyms] => Array
        (
        )

    [DAs] => Array
        (
        )

    [SignalingPathways] => Array
        (
        )

)
Links

Humpath: (empty)

thefetus.net: (empty)

eMedicine: (empty)

OMIM: (empty)

Wikipedia: (empty)

DiseaseDB: (empty)