Hypogonadotrophic hypogonadism

Symptom Information:

Symptom ID: HPO:0000044
Synonyms:
Hypogonadism, hypogonadotropic [HPO:0000044]
Isolated hypogonadotropic hypogonadism [HPO:0000044]
Hypogonadism, hypogonadotropic [OMIM:Hypogonadism, hypogonadotropic]
Hypogonadotrophic hypogonadism [OMIM:Hypogonadotrophic hypogonadism]
Isolated hypogonadotropic hypogonadism [OMIM:Isolated hypogonadotropic hypogonadism]
Hypogonadotropic hypogonadism [OMIM:Hypogonadotropic hypogonadism]
Hypogonadotropic hypogonadism (in some patients) [OMIM:Hypogonadotropic hypogonadism (in some patients)]
Hypogonadotropic hypogonadism (rare) [OMIM:Hypogonadotropic hypogonadism (rare)]
Quality:
Cross references:
OMIM: "Hypogonadism, hypogonadotropic" [OMIM:Hypogonadism, hypogonadotropic]
OMIM: "Hypogonadotrophic hypogonadism" [OMIM:Hypogonadotrophic hypogonadism]
OMIM: "Isolated hypogonadotropic hypogonadism" [OMIM:Isolated hypogonadotropic hypogonadism]
OMIM: "Hypogonadotropic hypogonadism" [OMIM:Hypogonadotropic hypogonadism]
OMIM: "Hypogonadotropic hypogonadism (in some patients)" [OMIM:Hypogonadotropic hypogonadism (in some patients)]
OMIM: "Hypogonadotropic hypogonadism (rare)" [OMIM:Hypogonadotropic hypogonadism (rare)]
Is a (Direct Parents):
HPO         Hypogonadism
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       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)
       Abnormality of the endocrine system(HPO:0000818)
          Puberty and gonadal disorders(HPO:0008373)
             Hypogonadism(HPO:0000135)
                Hypogonadotrophic hypogonadism(HPO:0000044)
MedDRA:
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)