Aplasia of the pectoralis major muscle

Symptom Information:

Symptom ID: HPO:0009751
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO         Pectoral muscle hypoplasia/aplasia
HPO         Aplasia of the musculature
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 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)
                               Aplasia of the pectoralis major muscle(HPO:0009751)
       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)
                      Aplasia of the pectoralis major muscle(HPO:0009751)
          Abnormality of muscle morphology(HPO:0011805)
             Aplasia/Hypoplasia involving the skeletal musculature(HPO:0001460)
                Aplasia of the musculature(HPO:0100854)
                   Aplasia of the pectoralis major muscle(HPO:0009751)
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

Acro-pectoro-renal dysplasia (Orphanet:956)
CHILD syndrome (Orphanet:139)
Carey-Fineman-Ziter syndrome (Orphanet:1358)
Holt-Oram syndrome (Orphanet:392)
Moebius syndrome (Orphanet:570)
Poland syndrome (Orphanet:2911)
Shoulder and girdle defects - familial intellectual deficit (Orphanet:2580)
Ulnar-mammary syndrome (Orphanet:3138)