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hemophilia A

Go to external page http://purl.obolibrary.org/obo/MONDO_0010602

The most common form of hemophilia characterized by spontaneous or prolonged hemorrhages due to factor VIII deficiency. [ Orphanet:98878 ]

Synonyms: hereditary Factor VIII deficiency factor VIII deficiency congenital factor VIII disorder hemophilia A hemophilia a, X-linked recessive Subhemophilia haemophilia a, X-linked recessive hemophilia type a hemophilia type A hereditary Factor VIII deficiency disease haemophilia type A haemophilia type a

This is just here as a test because I lose it

Term information

database cross reference
  • MedDRA:10016080 (Orphanet:98878/e)
  • UMLS:C0019069 (Orphanet:98878/e)
  • EFO:0007267 (MONDO:equivalentTo)
  • OMIM:306700 (Orphanet:98878/e)
  • OMIM:134500 (MONDO:equivalentTo)
  • DOID:0111823 (MONDO:mondoIsBroaderThanSource)
  • ICD9:286.0 (DOID:12134)
  • GARD:6591 (Orphanet:98878)
  • NCIT:C27146 (MONDO:equivalentTo)
  • Orphanet:98878 (OMIM:306700)
  • DOID:12134 (MONDO:equivalentTo)
  • SCTID:234440005 (MONDO:equivalentTo)
  • MESH:D006467 (Orphanet:98878/e)
  • NORD:1221 (MONDO:NORD)
Subsets

gard_rare, ordo_disease, rare, nord_rare, orphanet_rare, clingen

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/4521

closeMatch

http://identifiers.org/meddra/10016080

exactMatch

http://identifiers.org/snomedct/234440005

http://purl.obolibrary.org/obo/NCIT_C27146

http://identifiers.org/mesh/D006467

http://www.orpha.net/ORDO/Orphanet_98878

https://omim.org/entry/306700

http://linkedlifedata.com/resource/umls/id/C0019069

https://omim.org/entry/134500

http://purl.obolibrary.org/obo/DOID_12134

has related synonym

classical hemophilia

classic hemophilia

classic haemophilia

hemophilia, classic

haemophilia A, congenital

factor 8 deficiency

autosomal haemophilia a

HEMA

Haemophilia A

hemophilia A, congenital

hem A

autosomal hemophilia a

classical haemophilia

id

MONDO:0010602

narrowMatch

http://purl.obolibrary.org/obo/DOID_0111823

seeAlso

https://search.clinicalgenome.org/kb/conditions/MONDO:0010602