OBO ID: DOID:0080289
Term Name: orofaciodigital syndrome XVII Search Ontology:
Synonyms:
Definition: An orofaciodigital syndrome that has_material_basis_in homozygous mutation in the INTU gene on chromosome 4q28. https://pubmed.ncbi.nlm.nih.gov/23459408/
References:
Ontology: Human Disease   (DOID:0080289)
OTHER orofaciodigital syndrome XVII PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
INTU ?Orofaciodigital syndrome XVII 617926
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None