ZFIN Human Disease: hereditary mixed polyposis syndrome 2

OBO ID: DOID:0111686

Term Name:	hereditary mixed polyposis syndrome 2		Search Ontology:
Synonyms:	HMPS2
Definition:	A hereditary mixed polyposis syndrome that has_material_basis_in heterozygous mutation in the BMPR1A gene on chromosome 10q23.2. https://www.ncbi.nlm.nih.gov/pubmed/16525031
References:	OMIM:610069
Ontology:	Human Disease ( DOID:0111686 )

Relationships

is a type of:	autosomal dominant disease hereditary mixed polyposis syndrome autosomal dominant disease hereditary mixed polyposis syndrome Show first 5 Terms

OTHER hereditary mixed polyposis syndrome 2 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
BMPR1A	bmpr1ab bmpr1aa	Polyposis syndrome, hereditary mixed, 2	610069

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None