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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