Congenital posterior urethral valve
Symptom Information:
Symptom ID: | HPO:0010957 | ||||||||||||||||||
Synonyms: |
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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 valve(HPO:0010481) Congenital posterior urethral valve(HPO:0010957) 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 valve(HPO:0010481) Congenital posterior urethral valve(HPO:0010957) 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 valve(HPO:0010481) Congenital posterior urethral valve(HPO:0010957) MedDRA: Congenital, familial and genetic disorders(MedDRA:10010331) Renal and urinary tract disorders congenital(MedDRA:10038360) Renal and urinary tract disorders congenital NEC(MedDRA:10038361) Congenital posterior urethral valve(HPO:0010957) |
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Database Frequency: | 9 / 7739 | ||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Alström syndrome | (Orphanet:64) |
Bilateral renal agenesis | (Orphanet:1848) |
Floating-Harbor syndrome | (Orphanet:2044) |
Polycystic ovaries - urethral sphincter dysfunction | (Orphanet:2795) |
Prune belly syndrome | (Orphanet:2970) |
SILVER-RUSSELL SYNDROME | (OMIM:180860) |
Silver-Russell syndrome | (Orphanet:813) |
Townes-Brocks syndrome | (Orphanet:857) |
UROFACIAL SYNDROME 1 | (OMIM:236730) |