- OMIM ID
-
242150
- OMIM term:
- ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS
- Alternative terms:
-
KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL RECESSIVE
KID SYNDROME, AUTOSOMAL RECESSIVE
DESMONS SYNDROME
- (∗) Location:
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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