OBO ID: DOID:0111822
Term Name: CHILD syndrome Search Ontology:
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 )
OTHER CHILD syndrome PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
NSDHL CHILD syndrome 308050
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None