NPHP3-associated disease

DIS: 28




NPHP3-associated disease

Definition: (empty)


Synonyms:
There are no synonyms for this malformative disease.

Category: Monogenic disease

Developmental anomalies

Listed in the disease's profile :

Observed in MDB cases: (graph view)


There are no developmental anomalies for this disease.
Case records

Associated signaling pathways
Associations
Array
(
    [MalformativeDisease] => Array
        (
            [id] => 28
            [name] => NPHP3-associated disease
            [description] => 
            [category_id] => 2
            [gene_id] => 
            [chromosomal_anomaly_id] => 
            [infectious_agent_id] => 
            [toxic_agent_id] => 
            [maternal_condition_id] => 
            [omim_ref] => 
            [humpath_ref] => 14046
            [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
        (
            [0] => Array
                (
                    [id] => 433
                    [name] => Nephronophtisis
                    [description] => Nephronophthisis is a chronic tubulo-interstitial nephritis which progress to terminal renal failure.
                    [author_id] => 2
                    [topo_code] => 41
                    [category_code] => 0
                    [system_code] => 32
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 14044
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-07-17 18:26:57
                    [modified] => 2008-07-31 13:40:03
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                    [DiseasesAnomaly] => Array
                        (
                            [id] => 40
                            [disease_id] => 28
                            [anomaly_id] => 433
                        )

                )

            [1] => Array
                (
                    [id] => 434
                    [name] => Tapetoretinal degeneration
                    [description] => Degeneration of the pigmented layer of the retina. A hereditary disorder of the retina mainly affecting photoreceptors and retinal pigment epithelium; this may be a manifestation of Friedreich ataxia, Refsum disease, and abetalipoproteinemia. 

                    [author_id] => 2
                    [topo_code] => 50
                    [category_code] => 19
                    [system_code] => 51
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 14045
                    [omim_ref] => 272600
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-07-17 18:28:31
                    [modified] => 2008-12-17 15:10:20
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                    [DiseasesAnomaly] => Array
                        (
                            [id] => 41
                            [disease_id] => 28
                            [anomaly_id] => 434
                        )

                )

            [2] => Array
                (
                    [id] => 435
                    [name] => Congenital Hepatic Fibrosis,
                    [description] => Congenital hepatic fibrosis is an inherited fibrocystic liver disease associated with proliferation of interlobular bile ducts within the portal areas and fibrosis that do not alter hepatic lobular architecture. The fibrosis would affect resistance in portal veins leading to portal hypertension
                    [author_id] => 2
                    [topo_code] => 0
                    [category_code] => 9
                    [system_code] => 0
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 8684
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => Q44.6 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-07-17 18:29:42
                    [modified] => 2008-08-15 15:25:29
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                    [DiseasesAnomaly] => Array
                        (
                            [id] => 42
                            [disease_id] => 28
                            [anomaly_id] => 435
                        )

                )

        )

    [SignalingPathways] => Array
        (
        )

)
Links

Humpath: 14046

thefetus.net: (empty)

eMedicine: (empty)

OMIM: (empty)

Wikipedia: (empty)

DiseaseDB: (empty)