- OMIM ID
-
308050
- OMIM term:
- CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS
- Alternative terms:
-
CHILD SYNDROME
ICHTHYOSIFORM ERYTHRODERMA, UNILATERAL, WITH IPSILATERAL MALFORMATIONS, ESPECIALLY ABSENCE DEFORMITY OF LIMBS
- (∗) Location:
- Xq28
- (†) Associated OMIM genes:
- NSDHL
- (‡) Associated MGI genes:
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