Pectoralis hypoplasia

Symptom Information:

Symptom ID: HPO:0008998
Synonyms:
Pectoralis hypoplasia [OMIM:Pectoralis hypoplasia]
Quality:
Cross references:
OMIM: "Pectoralis hypoplasia" [OMIM:Pectoralis hypoplasia]
Is a (Direct Parents):
HPO         Pectoral muscle hypoplasia/aplasia
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)
                      Pectoralis hypoplasia(HPO:0008998)
       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)
                               Pectoralis hypoplasia(HPO:0008998)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Acro-renal-ocular syndrome (Orphanet:959)
Okihiro syndrome (Orphanet:93293)