Hypergonadotropic hypogonadism
Symptom Information:
Symptom ID: | HPO:0000815 | |||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the endocrine system(HPO:0000818) Puberty and gonadal disorders(HPO:0008373) Hypogonadism(HPO:0000135) Hypergonadotropic hypogonadism(HPO:0000815) Abnormality of the genitourinary system(HPO:0000119) Abnormality of the genital system(HPO:0000078) Abnormality of reproductive system physiology(HPO:0000080) Hypogonadism(HPO:0000135) Hypergonadotropic hypogonadism(HPO:0000815) MedDRA: Endocrine disorders(MedDRA:10014698) Endocrine disorders of gonadal function(MedDRA:10014701) Endocrine abnormalities of gonadal function NEC(MedDRA:10014691) Hypergonadotropic hypogonadism(HPO:0000815) |
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Database Frequency: | 48 / 7739 | |||||||||||||
Resource: |
All diseases associated with this symptom:
2p21 microdeletion syndrome | (Orphanet:163693) |
46,XY complete gonadal dysgenesis | (Orphanet:242) |
ALPHA-METHYLACYL-CoA RACEMASE DEFICIENCY | (OMIM:614307) |
Alopecia - intellectual deficit - hypergonadotropic hypogonadism | (Orphanet:1014) |
Alström syndrome | (Orphanet:64) |
Aromatase deficiency | (Orphanet:91) |
Atypical hypotonia - cystinuria syndrome | (Orphanet:238523) |
Autosomal dominant progressive external ophthalmoplegia | (Orphanet:254892) |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
CHONDRODYSPLASIA, ACROMESOMELIC, WITH GENITAL ANOMALIES | (OMIM:609441) |
Classic galactosemia | (Orphanet:79239) |
Congenital cataracts - facial dysmorphism - neuropathy | (Orphanet:48431) |
Congenital lactic acidosis, Saguenay-Lac-St. Jean type | (Orphanet:70472) |
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome | (Orphanet:2229) |
FANCONI ANEMIA, COMPLEMENTATION GROUP A | (OMIM:227650) |
FANCONI ANEMIA, COMPLEMENTATION GROUP C | (OMIM:227645) |
FANCONI ANEMIA, COMPLEMENTATION GROUP D2 | (OMIM:227646) |
FANCONI ANEMIA, COMPLEMENTATION GROUP E | (OMIM:600901) |
Faisalabad histiocytosis | (Orphanet:254707) |
Fanconi anemia | (Orphanet:84) |
H syndrome | (Orphanet:168569) |
Hypotonia - cystinuria syndrome | (Orphanet:163690) |
Infantile onset spinocerebellar ataxia | (Orphanet:1186) |
Intellectual deficit - dysmorphism - hypogonadism - diabetes mellitus | (Orphanet:3044) |
Leukoencephalopathy - dystonia - motor neuropathy | (Orphanet:163684) |
Leydig cell hypoplasia | (Orphanet:755) |
Leydig cell hypoplasia due to complete LH resistance | (Orphanet:96265) |
Leydig cell hypoplasia due to partial LH resistance | (Orphanet:96266) |
MACS syndrome | (Orphanet:217335) |
Male hypergonadotropic hypogonadism - intellectual deficit - skeletal anomalies | (Orphanet:2234) |
Marinesco-Sjögren syndrome | (Orphanet:559) |
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism | (Orphanet:280679) |
OVARIAN DYSGENESIS 2 | (OMIM:300510) |
Obesity due to leptin receptor gene deficiency | (Orphanet:179494) |
PMM2-CDG | (Orphanet:79318) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 1 | (OMIM:157640) |
Perrault Syndrome 1 | (OMIM:233400) |
Perrault Syndrome 3 | (OMIM:614129) |
Perrault Syndrome 5 | (OMIM:616138) |
Pigmented hypertrichosis with insulin dependent diabetes mellitus syndrome | (Orphanet:254723) |
Primary hypergonadotropic hypogonadism - partial alopecia | (Orphanet:2232) |
Progressive external ophthalmoplegia - myopathy - emaciation | (Orphanet:352447) |
Retinitis pigmentosa - intellectual deficit - deafness - hypogenitalism | (Orphanet:3085) |
Rosaï-Dorfman disease | (Orphanet:158014) |
TESTES, RUDIMENTARY | (OMIM:273150) |
Wolfram syndrome 1 | (OMIM:222300) |
Woodhouse-Sakati syndrome | (Orphanet:3464) |
Xq27.3q28 duplication syndrome | (Orphanet:261483) |