Human Disease Ontology 123

Last uploaded: September 28, 2023
Preferred Name

factor VII deficiency

Synonyms

deficiency, stable

Definitions

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.

ID

http://purl.obolibrary.org/obo/DOID_2215

database_cross_reference

GARD:2238

SNOMEDCT_US_2022_09_01:154820003

NCI:C131631

MESH:D005168

ICD10CM:D68.2

UMLS_CUI:C0015503

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.

disease has feature

http://purl.obolibrary.org/obo/DOID_801

has exact synonym

deficiency, stable

has material basis in

http://purl.obolibrary.org/obo/GENO_0000148

has symptom

http://purl.obolibrary.org/obo/SYMP_0000742

http://purl.obolibrary.org/obo/SYMP_0000007

http://purl.obolibrary.org/obo/SYMP_0000756

http://purl.obolibrary.org/obo/SYMP_0000448

has_obo_namespace

disease_ontology

id

DOID:2215

in_subset

http://purl.obolibrary.org/obo/doid#DO_rare_slim

http://purl.obolibrary.org/obo/doid#NCIthesaurus

label

factor VII deficiency

notation

DOID:2215

prefLabel

factor VII deficiency

subClassOf

http://purl.obolibrary.org/obo/DOID_1247

http://purl.obolibrary.org/obo/DOID_0050737

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/MTHU032016 Online Mendelian Inheritance in Man LOOM
http://purl.bioontology.org/ontology/MESH/D005168 Medical Subject Headings LOOM
http://purl.bioontology.org/ontology/OMIM/227500 Online Mendelian Inheritance in Man LOOM