Erectile abnormalities
Symptom Information:
Symptom ID: | HPO:0100639 | |||||||||||||||||||||||
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 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) Abnormality of the male genitalia(HPO:0010461) Abnormality of male external genitalia(HPO:0000032) Abnormality of the penis(HPO:0000036) Erectile abnormalities(HPO:0100639) MedDRA: |
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Database Frequency: | 15 / 7739 | |||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Acromegaly | (Orphanet:963) |
Adult polyglucosan body disease | (Orphanet:206583) |
Adult-onset autosomal dominant leukodystrophy | (Orphanet:99027) |
Castleman disease | (Orphanet:160) |
Cogan syndrome | (Orphanet:1467) |
Cushing syndrome | (Orphanet:553) |
Familial Dupuytren contracture | (Orphanet:79142) |
Fragile X-associated tremor/ataxia syndrome | (Orphanet:93256) |
Isolated spina bifida | (Orphanet:823) |
Kallmann syndrome | (Orphanet:478) |
Kennedy disease | (Orphanet:481) |
Norrie disease | (Orphanet:649) |
Scleroderma | (Orphanet:801) |
Systemic sclerosis | (Orphanet:90291) |
Whipple disease | (Orphanet:3452) |