Search Ontology:
Human Disease

CHILD syndrome

Term ID
DOID:0111822
Synonyms
  • CHILD nevus
  • congenital hemidysplasia with ichthyosiform nevus and limbs defects
Definition
A syndrome characterized by congenital hemidysplasia, ichythyosiform erythrodema, and limb defects that has_material_basis_in heterozygous mutation in the NSDHL gene on chromosome Xq28. https://www.ncbi.nlm.nih.gov/pubmed/7408908
References
Ontology
Human Disease   ( DOID:0111822 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models