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DO Term : hemophilia B [DOID:12259] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hemophilia that has_material_basis_in Factor IX deficiency, which makes coagulation much more prolonged. The disease is inherited as an X-linked recessive trait.

synonyms:
MESH:D002836,
Congenital factor IX deficiency,
NCI:C26721,
GARD:8732,
ICD10CM:D67,
ICD9CM:286.1,
UMLS_CUI:C0008533,
OMIM:306900,
306900,
Congenital factor IX disorder,
SNOMEDCT_US_2023_03_01:41788008,
factor IX deficiency,
deficiency, functional factor IX

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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