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MIM:308050 - CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS
Xenbase Genes: nsdhl
Human Disease Resource: MIM
MONDO:0010621 - CHILD syndrome |
DOID:0111822 - CHILD syndrome |
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MONDO:0010621 - CHILD syndrome |
DOID:0111822 - CHILD syndrome |