Human genes for CHILD syndrome
CHILD syndrome [DOID:0111822]
A syndrome characterized by congenital hemidysplasia, ichythyosiform erythrodema, and limb defects that has_material_basis_in heterozygous mutation in NSDHL on chromosome Xq28.
Synonyms: CHILD syndrome, CHILD disease, CHILD disorder, CHILD syndromes, DOID:0111822 ...