Abnormality of the sternum

Symptom Information:

Symptom ID: HPO:0000766
Synonyms:
Pectus carinatum or pectus excavatum [HPO:0000766]
Pectus deformities [HPO:0000766]
Pectus deformity [HPO:0000766]
Pectus excavatum or carinatum [HPO:0000766]
Pectus excavatum or pectus carinatum [HPO:0000766]
Pectus excavatum/carinatum [HPO:0000766]
Sternal anomalies [HPO:0000766]
Sternum anomaly [Orphanet:15600]
Congenital malformation of sternum (disorder) [Orphanet:15600]
Congenital malformation of sternum [Orphanet:15600]
Pectus carinatum or pectus excavatum [OMIM:Pectus carinatum or pectus excavatum]
Pectus deformities [OMIM:Pectus deformities]
Pectus deformity [OMIM:Pectus deformity]
Pectus excavatum or carinatum [OMIM:Pectus excavatum or carinatum]
Sternal anomalies [OMIM:Sternal anomalies]
Sternal/sternum anomalies [Orphanet:15600]
Pectus deformities (in some patients) [OMIM:Pectus deformities (in some patients)]
Quality:
Cross references:
Orphanet:15600 "Sternal/sternum anomalies" [Orphanet:15600]
OMIM: "Pectus carinatum or pectus excavatum" [OMIM:Pectus carinatum or pectus excavatum]
OMIM: "Pectus deformities" [OMIM:Pectus deformities]
OMIM: "Pectus deformity" [OMIM:Pectus deformity]
OMIM: "Pectus excavatum or carinatum" [OMIM:Pectus excavatum or carinatum]
OMIM: "Sternal anomalies" [OMIM:Sternal anomalies]
OMIM: "Pectus deformities (in some patients)" [OMIM:Pectus deformities (in some patients)]
UMLS:C0432176 "Congenital malformation of sternum" [Orphanet:15600]
Is a (Direct Parents):
Orphanet Abnormality of the thorax
HPO         Abnormality of the thorax
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:
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)