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DO Term : congenital afibrinogenemia [DOID:2236] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A blood coagulation disease that is characterized by an impaired blood clotting resulting from a lack deficiency of a the fibrinogen protein (coagulation factor I).

synonyms:
Factor I deficiency,
Fibrinogen deficiency,
OMIM:202400,
MESH:D000347,
GARD:5761,
NCI:C98130,
202400,
UMLS_CUI:C0001733,
SNOMEDCT_US_2023_03_01:278504009

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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