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Hemophilia A (MONDO:0010602)

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The most common form of hemophilia characterized by spontaneous or prolonged hemorrhages due to factor VIII deficiency.

Overview

Category

hematologic disorder

Ontology ID

MONDO:0010602

Internal:11751

Synonyms

congenital factor VIII disorder

factor VIII deficiency

haemophilia a, X-linked recessive

haemophilia type A

haemophilia type a

hemophilia A

hemophilia a, X-linked recessive

hemophilia type A

hemophilia type a

hereditary Factor VIII deficiency

hereditary Factor VIII deficiency disease

HEMA

Haemophilia A

autosomal haemophilia a

autosomal hemophilia a

classic haemophilia

classic hemophilia

classical haemophilia

classical hemophilia

factor 8 deficiency

haemophilia A, congenital

hem A

hemophilia A, congenital

hemophilia, classic

Mapped terms

DOID:12134

GARD:0006591

ICD10CM:D66

ICD9:286.0

MEDGEN:5501

MESH:D006467

MedDRA:10016080

NANDO:2200676

NCIT:C27146

NORD:1221

OMIM:134500

OMIM:306700

Orphanet:98878

SCTID:234440005

UMLS:C0019069

icd11.foundation:337607970

Child terms

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