Impotence
Symptom Information:
Symptom ID: | HPO:0000802 | ||||||||||||||||||||||||||||
Synonyms: |
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Quality: | |||||||||||||||||||||||||||||
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 genitourinary system(HPO:0000119) Abnormality of the genital system(HPO:0000078) Abnormality of reproductive system physiology(HPO:0000080) Impotence(HPO:0000802) Abnormal genital system morphology(HPO:0012243) 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) 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) MedDRA: |
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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) |