Abnormality of the sternum
Symptom Information:
Symptom ID: | HPO:0000766 | |||||||||||||||||
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 skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormal axial skeleton morphology(HPO:0009121) Abnormality of the thorax(HPO:0000765) Abnormality of the sternum(HPO:0000766) MedDRA: |
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Database Frequency: | 31 / 7739 | |||||||||||||||||
Resource: |
All diseases associated with this symptom:
Alpha-mannosidosis | (Orphanet:61) |
Aneurysm - osteoarthritis syndrome | (Orphanet:284984) |
Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
C syndrome | (Orphanet:1308) |
CARDIOFACIOCUTANEOUS SYNDROME 4 | (OMIM:615280) |
Cantrell pentalogy | (Orphanet:1335) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Craniosynostosis - fibular aplasia | (Orphanet:1533) |
Gaucher disease type 3 | (Orphanet:77261) |
Gorlin syndrome | (Orphanet:377) |
Holt-Oram syndrome | (Orphanet:392) |
Jeune syndrome | (Orphanet:474) |
LEOPARD SYNDROME 2 | (OMIM:611554) |
LOEYS-DIETZ SYNDROME 1 | (OMIM:609192) |
LOEYS-DIETZ SYNDROME 2 | (OMIM:610168) |
LOEYS-DIETZ SYNDROME 4 | (OMIM:614816) |
Legius syndrome | (Orphanet:137605) |
Loeys-Dietz syndrome type 1 | (Orphanet:60030) |
MACS syndrome | (Orphanet:217335) |
MASS SYNDROME | (OMIM:604308) |
Marden-Walker syndrome | (Orphanet:2461) |
NOONAN SYNDROME 5 | (OMIM:611553) |
OPITZ-KAVEGGIA SYNDROME | (OMIM:305450) |
PHACE syndrome | (Orphanet:42775) |
PSEUDOXANTHOMA ELASTICUM, FORME FRUSTEPSEUDOXANTHOMA ELASTICUM, HETEROZYGOUS, INCLUDED | (OMIM:177850) |
Poland syndrome | (Orphanet:2911) |
Pseudoxanthoma elasticum | (Orphanet:758) |
Recombinant 8 syndrome | (Orphanet:96167) |
Rubinstein-Taybi syndrome due to CREBBP mutations | (Orphanet:353277) |
VACTERL/VATER association | (Orphanet:887) |
Yunis-Varon syndrome | (Orphanet:3472) |