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hemophilia B

Go to external page http://purl.obolibrary.org/obo/MONDO_0010604

Hemophilia B is a form of hemophilia characterized by spontaneous or prolonged hemorrhages due to factor IX deficiency. [ Orphanet:98879 ]

Synonyms: hereditary Factor IX deficiency disease hereditary Factor IX deficiency congenital factor IX deficiency congenital factor IX disorder factor IX deficiency hemophilia B Christmas disease hemophilia b, X-linked recessive haemophilia b, X-linked recessive hemophilia type B haemophilia type B deficiency, functional factor IX

This is just here as a test because I lose it

Term information

database cross reference
  • OMIM:306900 (Orphanet:98879/e)
  • MedDRA:10016077 (Orphanet:98879/e)
  • NCIT:C26721 (MONDO:equivalentTo)
  • DOID:12259 (MONDO:equivalentTo)
  • EFO:0009154 (MONDO:equivalentTo)
  • SCTID:41788008 (MONDO:equivalentTo)
  • GARD:8732 (Orphanet:98879)
  • ICD9:286.1 (MONDO:i2s)
  • MESH:D002836 (Orphanet:98879/e)
  • NORD:1222 (MONDO:NORD)
  • Orphanet:98879 (OMIM:306900)
  • UMLS:C0008533 (Orphanet:98879/e)
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/10016077

exactMatch

http://identifiers.org/snomedct/41788008

https://omim.org/entry/306900

http://www.orpha.net/ORDO/Orphanet_98879

http://purl.obolibrary.org/obo/NCIT_C26721

http://linkedlifedata.com/resource/umls/id/C0008533

http://identifiers.org/mesh/D002836

http://purl.obolibrary.org/obo/DOID_12259

has related synonym

haemophilia B(M)

HEMB

F9 deficiency

hemophilia B Leyden

haemophilia B Leyden

factor 9 deficiency

hem B

plasma thromboplastin component deficiency

hemophilia B(M)

id

MONDO:0010604

seeAlso

https://search.clinicalgenome.org/kb/conditions/MONDO:0010604

https://rarediseases.info.nih.gov/diseases/8732/hemophilia-b