JSON

dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome

^ http://purl.obolibrary.org/obo/MONDO_0008915

A syndrome is characterized by the association of dilated cardiomyopathy and hypergonadotropic hypogonadism (DCM-HH). [ Orphanet:2229 ]

Term info

database cross reference
  • UMLS:C0796031 (Orphanet:2229/e)
  • NCIT:C174217 (MONDO:equivalentTo)
  • UMLS:C0796083 (Orphanet:2229/e)
  • Orphanet:2229 (OMIM:212112)
  • SCTID:719451006 (MONDO:equivalentTo)
  • OMIM:212112 (Orphanet:2229/e)
  • GARD:0003373 (MONDO:equivalentTo)
  • DOID:0111584 (MONDO:equivalentTo)
Subsets

ordo_malformation_syndrome

definition

A syndrome is characterized by the association of dilated cardiomyopathy and hypergonadotropic hypogonadism (DCM-HH).

exactMatch

http://linkedlifedata.com/resource/umls/id/C0796083, http://purl.obolibrary.org/obo/NCIT_C174217, http://purl.obolibrary.org/obo/Orphanet_2229, http://purl.obolibrary.org/obo/DOID_0111584, http://identifiers.org/snomedct/719451006, http://linkedlifedata.com/resource/umls/id/C0796031, https://omim.org/entry/212112

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0016337

has exact synonym

Malouf syndrome, cardiogenital syndrome, Najjar syndrome

has related synonym

cardiomyopathy, congestive, with hypergonadotropic hypogonadism, cardiomyopathy, dilated, with hypergonadotropic hypogonadism, cardiomyopathy with primary testicular failure, dilated cardiomyopathy with hypergonadotropic hypogonadism, cardiomyopathy, dilated, with premature ovarian failure, genital anomaly with cardiomyopathy

id

MONDO:0008915