Sirenomelia
Symptom Information:
Symptom ID: | HPO:0010497 | |||||||||||
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 skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormal appendicular skeleton morphology(HPO:0011844) Abnormality of limb bone morphology(HPO:0002813) Abnormality of the lower limb(HPO:0002814) Sirenomelia(HPO:0010497) MedDRA: Renal and urinary disorders(MedDRA:10038359) Genitourinary tract disorders NEC(MedDRA:10018188) Congenital genitourinary tract anomalies NEC(MedDRA:10010484) Sirenomelia(HPO:0010497) |
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Database Frequency: | 6 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
Bilateral renal agenesis | (Orphanet:1848) |
Craniorachischisis | (Orphanet:63260) |
Diabetic embryopathy | (Orphanet:1926) |
Proteus syndrome | (Orphanet:744) |
Renal dysplasia - megalocystis - sirenomelia | (Orphanet:1850) |
Sirenomelia | (Orphanet:3169) |