Sirenomelia

Symptom Information:

Symptom ID: HPO:0010497
Synonyms:
Sympodia [HPO:0010497]
Sirenomelia sequence [HPO:0010497]
Sirenomelia sequence (disorder) [Orphanet:21040]
Mermaid sirenomelia (disorder) [Orphanet:21040]
Sirenoform monster (disorder) [Orphanet:21040]
Sirenomelia [Orphanet:21040]
Sirenomelia/mermaid/lower limb fusion [Orphanet:21040]
Sympodia [Orphanet:21040]
Sirenomelia [MedDRA:10072457]
Sympodia [MedDRA:10072457]
Mermaid syndrome [MedDRA:10072457]
Quality:
Cross references:
Orphanet:21040 "Sirenomelia/mermaid/lower limb fusion" [Orphanet:21040]
UMLS:C0037205 "Sirenomelia" [HPO:0010497]
UMLS:C0037205 "Sirenomelia" [Orphanet:21040]
Is a (Direct Parents):
HPO         Abnormality of the lower limb
Orphanet Abnormality of the lower limb
MedDRA Congenital genitourinary tract anomalies NEC
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)
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)