Pectoral muscle hypoplasia/aplasia

Symptom Information:

Symptom ID: HPO:0005258
Synonyms:
Pectoral muscle absence [Orphanet:15560]
Absent pectoral muscles [Orphanet:15560]
Pectoral muscle hypoplasia/aplasia (Poland syndrome) [OMIM:Pectoral muscle hypoplasia/aplasia (Poland syndrome)]
Quality:
Cross references:
Orphanet:15560 "Absent pectoral muscles" [Orphanet:15560]
OMIM: "Pectoral muscle hypoplasia/aplasia (Poland syndrome)" [OMIM:Pectoral muscle hypoplasia/aplasia (Poland syndrome)]
Is a (Direct Parents):
HPO         Abnormality of the shoulder girdle musculature
Orphanet Abnormality of the thorax
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of the musculature of the limbs(HPO:0009127)
             Abnormality of the musculature of the upper limbs(HPO:0001446)
                Abnormality of the shoulder girdle musculature(HPO:0001435)
                   Pectoral muscle hypoplasia/aplasia(HPO:0005258)
       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 musculature of the limbs(HPO:0009127)
                      Abnormality of the musculature of the upper limbs(HPO:0001446)
                         Abnormality of the shoulder girdle musculature(HPO:0001435)
                            Pectoral muscle hypoplasia/aplasia(HPO:0005258)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Frontonasal dysplasia (Orphanet:250)