Urethral stenosis
Symptom Information:
Symptom ID: | HPO:0008661 | |||||||||||||||||||||
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 urinary system(HPO:0000079) Abnormality of the lower urinary tract(HPO:0010936) Abnormality of the urethra(HPO:0000795) Urethral obstruction(HPO:0000796) Urethral stenosis(HPO:0008661) 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 urethra(HPO:0000795) Urethral obstruction(HPO:0000796) Urethral stenosis(HPO:0008661) Abnormality of the male genitalia(HPO:0010461) Abnormality of male external genitalia(HPO:0000032) Abnormality of the urethra(HPO:0000795) Urethral obstruction(HPO:0000796) Urethral stenosis(HPO:0008661) MedDRA: Renal and urinary disorders(MedDRA:10038359) Urethral disorders (excl calculi)(MedDRA:10046447) Structural and obstructive urethral disorders (excl congenital)(MedDRA:10042256) Urethral stenosis(HPO:0008661) |
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Database Frequency: | 9 / 7739 | |||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
17q12 microdeletion syndrome | (Orphanet:261265) |
Alström syndrome | (Orphanet:64) |
Bilateral renal agenesis | (Orphanet:1848) |
Diabetic embryopathy | (Orphanet:1926) |
Epidermolysis bullosa simplex with muscular dystrophy | (Orphanet:257) |
Hoyeraal-Hreidarsson syndrome | (Orphanet:3322) |
MACS syndrome | (Orphanet:217335) |
Polycystic ovaries - urethral sphincter dysfunction | (Orphanet:2795) |
Williams syndrome | (Orphanet:904) |