Disease #07108 (DCIDP (deafness, cataract, impaired intellectual development, polyneuropathy), OMIM:619354)

Official abbreviation DCIDP
Name deafness, cataract, impaired intellectual development, polyneuropathy
OMIM ID 619354
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene PSMC3
Associated tissues -
Disease features -
Remarks -
Date created 2024-10-24 10:04:46 +02:00 (CEST)
Date last edited N/A

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