ZFIN Human Disease: orofaciodigital syndrome XVII

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:	OMIM:617926
Ontology:	Human Disease ( DOID:0080289 )

Relationships

is a type of:	autosomal recessive disease orofaciodigital syndrome autosomal recessive disease orofaciodigital syndrome Show first 5 Terms

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Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
INTU	intu	?Orofaciodigital syndrome XVII	617926

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None