Hypogonadotrophic hypogonadism
Symptom Information:
Symptom ID: | HPO:0000044 | ||||||||
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) Hypogonadotrophic hypogonadism(HPO:0000044) Abnormality of the genitourinary system(HPO:0000119) Abnormality of the genital system(HPO:0000078) Abnormality of reproductive system physiology(HPO:0000080) Hypogonadism(HPO:0000135) Hypogonadotrophic hypogonadism(HPO:0000044) MedDRA: |
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Database Frequency: | 56 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
ADRENAL HYPOPLASIA, CONGENITAL | (OMIM:300200) |
ANE syndrome | (Orphanet:157954) |
Alström syndrome | (Orphanet:64) |
Anophthalmia/microphthalmia - esophageal atresia | (Orphanet:77298) |
Ataxia - hypogonadism - choroidal dystrophy | (Orphanet:1180) |
Brachytelephalangy - dysmorphism - Kallmann syndrome | (Orphanet:1295) |
CHARGE syndrome | (Orphanet:138) |
Cataract - intellectual deficit - hypogonadism | (Orphanet:1387) |
Cerebellar ataxia - hypogonadism | (Orphanet:1173) |
Congenital cataracts - facial dysmorphism - neuropathy | (Orphanet:48431) |
Cytomegalic congenital adrenal hypoplasia | (Orphanet:95702) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 | (OMIM:129900) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 | (OMIM:604292) |
EEC syndrome | (Orphanet:1896) |
EUNUCHOIDISM, FAMILIAL HYPOGONADOTROPIC | (OMIM:227200) |
Faisalabad histiocytosis | (Orphanet:254707) |
GORDON HOLMES SYNDROME | (OMIM:212840) |
H syndrome | (Orphanet:168569) |
HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA | (OMIM:308700) |
HYPOGONADOTROPIC HYPOGONADISM 10 WITH OR WITHOUT ANOSMIA | (OMIM:614839) |
HYPOGONADOTROPIC HYPOGONADISM 11 WITH OR WITHOUT ANOSMIA | (OMIM:614840) |
HYPOGONADOTROPIC HYPOGONADISM 12 WITH OR WITHOUT ANOSMIA | (OMIM:614841) |
HYPOGONADOTROPIC HYPOGONADISM 13 WITH OR WITHOUT ANOSMIA | (OMIM:614842) |
HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA | (OMIM:147950) |
HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA | (OMIM:244200) |
HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA | (OMIM:610628) |
HYPOGONADOTROPIC HYPOGONADISM 5 WITH OR WITHOUT ANOSMIA | (OMIM:612370) |
HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA | (OMIM:612702) |
HYPOGONADOTROPIC HYPOGONADISM 7 WITH OR WITHOUT ANOSMIA | (OMIM:146110) |
HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA | (OMIM:614837) |
HYPOGONADOTROPIC HYPOGONADISM 9 WITH OR WITHOUT ANOSMIA | (OMIM:614838) |
Hemochromatosis type 2 | (Orphanet:79230) |
Hemochromatosis type 3 | (Orphanet:225123) |
Hemochromatosis, type 1 | (OMIM:235200) |
Hemochromatosis, type 2A | (OMIM:602390) |
Hemochromatosis, type 2B | (OMIM:613313) |
ICHTHYOSIS AND MALE HYPOGONADISMRUD SYNDROME, INCLUDED | (OMIM:308200) |
Intellectual deficit - myopathy - short stature - endocrine defect | (Orphanet:3068) |
KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA | (OMIM:308750) |
Kallmann syndrome | (Orphanet:478) |
LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM | (OMIM:614381) |
Leukoencephalopathy - ataxia - hypodontia - hypomyelination | (Orphanet:137639) |
MELAS | (Orphanet:550) |
Moebius syndrome | (Orphanet:570) |
Mulibrey nanism | (Orphanet:2576) |
Neuroectodermal syndrome, Johnson type | (Orphanet:2316) |
Normosmic congenital hypogonadotropic hypogonadism | (Orphanet:432) |
Obesity due to prohormone convertase I deficiency | (Orphanet:71528) |
Odontoleukodystrophy | (Orphanet:77295) |
PGM1-CDG | (Orphanet:319646) |
Pigmented hypertrichosis with insulin dependent diabetes mellitus syndrome | (Orphanet:254723) |
Prader-Willi syndrome | (Orphanet:739) |
Roifman syndrome | (Orphanet:353298) |
Rosaï-Dorfman disease | (Orphanet:158014) |
Trichomegaly - retina pigmentary degeneration - dwarfism | (Orphanet:3363) |
Woodhouse-Sakati syndrome | (Orphanet:3464) |