OBO ID: DOID:0111822 |
Term Name: | CHILD syndrome | Search Ontology: | |
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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 | ||
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Ontology: | Human Disease ( DOID:0111822 ) |
OTHER CHILD syndrome PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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