ZFIN Human Disease: factor VII deficiency

OBO ID: DOID:2215

Term Name:	factor VII deficiency		Search Ontology:
Synonyms:	deficiency, stable
Definition:	A blood coagulation disease that is characterized by easy bleeding, has_symptom epistaxis, bleeding of the gums, menorrhagia, and occasionally hemarthrosis, and has_material_basis_in autosomal recessive inheritance of mutation in the F7 gene, which encodes coagulation factor VII, an important factor in the clotting cascade. (2)
References:	GARD:2238 ICD10CM:D68.2 MESH:D005168 NCI:C131631 OMIM:227500 ORDO:327 SNOMEDCT_US_2023_03_01:154820003 UMLS_CUI:C0015503
Ontology:	Human Disease ( DOID:2215 )

Relationships

is a type of:	autosomal recessive disease blood coagulation disease autosomal recessive disease blood coagulation disease Show first 5 Terms

OTHER factor VII deficiency PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
F7	f7	Factor VII deficiency	227500

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None