MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
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Parent Node:
expandcongenital hypogonadotropic hypogonadism (MONDO:0015770)
..Starting node
..expandrare disorder with congenital hypogonadotropic hypogonadism ()

       Child Nodes:
........expandANE syndrome ()
........expandataxia-hypogonadism-choroidal dystrophy syndrome ()
........expandBardet-Biedl syndrome ()
........expandbrachytelephalangy-dysmorphism-Kallmann syndrome ()
........expandcataract-intellectual disability-hypogonadism syndrome ()
........expandcerebellar ataxia-hypogonadism syndrome ()
........expandCHARGE syndrome ()
........expandhypogonadotropic hypogonadism 7 with or without anosmia ()
........expandhypogonadotropic hypogonadism-frontoparietal alopecia syndrome ()
........expandhypogonadotropic hypogonadism-retinitis pigmentosa syndrome ()
........expandhypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome ()
........expandhypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome ()
........expandhyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome ()
........expandKallmann syndrome-heart disease syndrome ()
........expandLaurence-Moon syndrome ()
........expandMoebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome ()
........expandpolyendocrine-polyneuropathy syndrome ()
........expandPrader-Willi syndrome ()
........expandPrader-Willi-like syndrome ()
........expandsickle cell anemia ()
........expandWoodhouse-Sakati syndrome ()



 Sister Nodes: 
..expandhypogonadotropic hypogonadism associated with other endocrinopathies ()
..expandisolated congenital hypogonadotropic hypogonadism ()
..expandrare disorder with congenital hypogonadotropic hypogonadism ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:15890
Name:rare disorder with congenital hypogonadotropic hypogonadism
Definition:
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:rare disorder with hypogonadotropic hypogonadism; rare disorder with secondary hypogonadism
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
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