Impotence

Symptom Information:

Symptom ID: HPO:0000802
Synonyms:
Erectile dysfunction [HPO:0000802]
Sexual impotence [Orphanet:40810]
Male erectile disorder (disorder) [Orphanet:40810]
Impotence (disorder) [Orphanet:40810]
impotence [HPO:0000802]
Erectile dysfunction [Orphanet:40810]
Erectile dysfunction [OMIM:Erectile dysfunction]
Impotence [OMIM:Impotence]
Impotence/painful erection/priapism/erection troubles [Orphanet:40810]
Erectile dysfunction [MedDRA:10061461]
Erectile disturbance [MedDRA:10061461]
Erection decreased [MedDRA:10061461]
Erection failure [MedDRA:10061461]
Erection inadequate [MedDRA:10061461]
Frigidity and impotence [MedDRA:10061461]
Impotence [MedDRA:10061461]
Impotent [MedDRA:10061461]
Impotentia erigendi [MedDRA:10061461]
Inability to maintain erection [MedDRA:10061461]
Male erectile disorder [MedDRA:10061461]
Male erectile disturbance due to general medical condition [MedDRA:10061461]
Impotence aggravated [MedDRA:10061461]
Erectile dysfunction NOS [MedDRA:10061461]
Potency disturbance [MedDRA:10061461]
Decreased frequency of erections [MedDRA:10061461]
Painful erection [MedDRA:10056303]
Painful penile erection (finding) [Orphanet:40810]
Painful penile erection [Orphanet:40810]
Quality:
Cross references:
HPO:0008652 "Autonomic erectile dysfunction" [Orphanet:40810]
Orphanet:40810 "Impotence/painful erection/priapism/erection troubles" [Orphanet:40810]
OMIM: "Erectile dysfunction" [OMIM:Erectile dysfunction]
OMIM: "Impotence" [OMIM:Impotence]
UMLS:C2187990 "impotence" [HPO:0000802]
UMLS:C0242350 "Erectile dysfunction" [Orphanet:40810]
UMLS:C0233973 "Painful penile erection" [Orphanet:40810]
Is a (Direct Parents):
MedDRA Sexual arousal disorders
HPO         Erectile abnormalities
Orphanet Functional anomalies of the genital system
HPO         Abnormality of reproductive system physiology
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)
             Abnormal genital system morphology(HPO:0012243)
                Abnormal external genitalia(HPO:0000811)
                   Abnormality of male external genitalia(HPO:0000032)
                      Abnormality of the penis(HPO:0000036)
                         Erectile abnormalities(HPO:0100639)
                            Impotence(HPO:0000802)
                Abnormality of the male genitalia(HPO:0010461)
                   Abnormality of male external genitalia(HPO:0000032)
                      Abnormality of the penis(HPO:0000036)
                         Erectile abnormalities(HPO:0100639)
                            Impotence(HPO:0000802)
             Abnormality of reproductive system physiology(HPO:0000080)
                Impotence(HPO:0000802)
MedDRA:
Database Frequency: 20 / 7739
Resource:

All diseases associated with this symptom:

ATTRV122I amyloidosis (Orphanet:85451)
Adrenomyeloneuropathy (Orphanet:139399)
Adult-onset autosomal dominant leukodystrophy (Orphanet:99027)
Cushing syndrome (Orphanet:553)
Familial amyloid polyneuropathy (Orphanet:85447)
Fragile X-associated tremor/ataxia syndrome (Orphanet:93256)
Hemochromatosis type 3 (Orphanet:225123)
Hemochromatosis type 4 (Orphanet:139491)
Hemochromatosis, type 1 (OMIM:235200)
Hemochromatosis, type 2A (OMIM:602390)
Hereditary sensory and autonomic neuropathy type 1B (Orphanet:139564)
Leber plus disease (Orphanet:99718)
MOYAMOYA DISEASE 6 WITH ACHALASIA (OMIM:615750)
Multiple system atrophy (Orphanet:102)
Sandhoff disease (Orphanet:796)
Sandhoff disease, adult form (Orphanet:309169)
Sandhoff disease, infantile form (Orphanet:309155)
Sandhoff disease, juvenile form (Orphanet:309162)
Steinert myotonic dystrophy (Orphanet:273)
X-linked cerebral adrenoleukodystrophy (Orphanet:139396)