ZFIN Human Disease: familial adenomatous polyposis 3

OBO ID: DOID:0080411

Term Name:	familial adenomatous polyposis 3		Search Ontology:
Synonyms:
Definition:	A familial adenomatous polyposis that has_material_basis_in homozygous or compound heterozygous mutation in the NTHL1 gene on chromosome 16p13. https://www.ncbi.nlm.nih.gov/pubmed/25938944
References:	OMIM:616415
Ontology:	Human Disease ( DOID:0080411 )

Relationships

is a type of:	autosomal recessive disease familial adenomatous polyposis autosomal recessive disease familial adenomatous polyposis Show first 5 Terms

OTHER familial adenomatous polyposis 3 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
NTHL1	nthl1	Familial adenomatous polyposis 3	616415

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None