Short sternum

Symptom Information:

Symptom ID: HPO:0000879
Synonyms:
Hypoplastic sternum [HPO:0000879]
Short sternum [OMIM:Short sternum]
Quality:
Cross references:
OMIM: "Short sternum" [OMIM:Short sternum]
Is a (Direct Parents):
HPO         Aplasia/Hypoplasia of the sternum
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)
                      Aplasia/Hypoplasia of the sternum(HPO:0006714)
                         Short sternum(HPO:0000879)
                   Aplasia/Hypoplasia involving bones of the thorax(HPO:0006711)
                      Aplasia/Hypoplasia of the sternum(HPO:0006714)
                         Short sternum(HPO:0000879)
                Aplasia/hypoplasia affecting bones of the axial skeleton(HPO:0009122)
                   Aplasia/Hypoplasia involving bones of the thorax(HPO:0006711)
                      Aplasia/Hypoplasia of the sternum(HPO:0006714)
                         Short sternum(HPO:0000879)
             Aplasia/hypoplasia involving the skeleton(HPO:0009115)
                Aplasia/hypoplasia affecting bones of the axial skeleton(HPO:0009122)
                   Aplasia/Hypoplasia involving bones of the thorax(HPO:0006711)
                      Aplasia/Hypoplasia of the sternum(HPO:0006714)
                         Short sternum(HPO:0000879)
MedDRA:
Database Frequency: 16 / 7739
Resource:

All diseases associated with this symptom:

COFFIN-SIRIS SYNDROME (OMIM:135900)
Coffin-Siris syndrome (Orphanet:1465)
Cornelia de Lange syndrome (Orphanet:199)
Dysosteosclerosis (Orphanet:1782)
MOMO syndrome (Orphanet:2563)
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1 (OMIM:257300)
MULTIPLE SYNOSTOSES SYNDROME 1 (OMIM:186500)
Marshall-Smith syndrome (Orphanet:561)
Mosaic variegated aneuploidy syndrome (Orphanet:1052)
Multiple synostoses syndrome (Orphanet:3237)
Orofaciodigital syndrome type 3 (Orphanet:2752)
SCARF syndrome (Orphanet:3134)
STERNUM, PREMATURE OBLITERATION OF SUTURES OF (OMIM:184800)
Schinzel-Giedion syndrome (Orphanet:798)
TARP syndrome (Orphanet:2886)
Ulbright-Hodes syndrome (Orphanet:3404)