Disease #01403 (KIDAD (keratitis-ichthyosis-deafness syndrome, autosomal dominant), OMIM:148210)
Official abbreviation |
KIDAD |
Name |
keratitis-ichthyosis-deafness syndrome, autosomal dominant |
OMIM ID |
148210 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
3 |
Phenotype entries for this disease |
3 |
Associated with 1 gene |
GJB2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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