Bowed humerus

Symptom Information:

Symptom ID: HPO:0003865
Synonyms:
Bowing of the humerus [HPO:0003865]
Humeral bowing [HPO:0003865]
Humeral bowing [OMIM:Humeral bowing]
Bowed humeri [OMIM:Bowed humeri]
Quality:
Cross references:
OMIM: "Humeral bowing" [OMIM:Humeral bowing]
OMIM: "Bowed humeri" [OMIM:Bowed humeri]
Is a (Direct Parents):
HPO         Bowing of the arm
HPO         Abnormality of the humerus
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)
             Abnormality of long bone morphology(HPO:0011314)
                Abnormal diaphysis morphology(HPO:0000940)
                   Anomaly of the limb diaphyses(HPO:0006504)
                      Bowing of the long bones(HPO:0006487)
                         Bowing of the arm(HPO:0006488)
                            Bowed humerus(HPO:0003865)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of the upper limb(HPO:0002817)
                      Abnormality of the upper arm(HPO:0001454)
                         Abnormality of the humerus(HPO:0003063)
                            Bowed humerus(HPO:0003865)
                      Bowing of the arm(HPO:0006488)
                         Bowed humerus(HPO:0003865)
                   Anomaly of the limb diaphyses(HPO:0006504)
                      Bowing of the long bones(HPO:0006487)
                         Bowing of the arm(HPO:0006488)
                            Bowed humerus(HPO:0003865)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Kyphomelic dysplasia (Orphanet:1801)
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I (OMIM:210710)
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 (Orphanet:2636)
Perinatal lethal hypophosphatasia (Orphanet:247623)
Spondylometaphyseal dysplasia, Schmidt type (Orphanet:93316)