Decreased hip abduction

Symptom Information:

Symptom ID: HPO:0003184
Synonyms:
Limited hip abduction [HPO:0003184]
Decreased hip abduction [OMIM:Decreased hip abduction]
Limited hip abduction [OMIM:Limited hip abduction]
Limited hip abduction (less than 10 degrees by age 12 months) [OMIM:Limited hip abduction (less than 10 degrees by age 12 months)]
Quality:
Cross references:
OMIM: "Decreased hip abduction" [OMIM:Decreased hip abduction]
OMIM: "Limited hip abduction" [OMIM:Limited hip abduction]
OMIM: "Limited hip abduction (less than 10 degrees by age 12 months)" [OMIM:Limited hip abduction (less than 10 degrees by age 12 months)]
Is a (Direct Parents):
HPO         Limited hip movement
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 pelvic girdle bone morphology(HPO:0002644)
                   Limited hip movement(HPO:0008800)
                      Decreased hip abduction(HPO:0003184)
             Abnormal joint morphology(HPO:0001367)
                Abnormality of joint mobility(HPO:0011729)
                   Limitation of joint mobility(HPO:0001376)
                      Limited hip movement(HPO:0008800)
                         Decreased hip abduction(HPO:0003184)
MedDRA:
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

ARTHROGRYPOSIS, DISTAL, TYPE 1A (OMIM:108120)
CHST3-related skeletal dysplasia (Orphanet:263463)
Digitotalar dysmorphism (Orphanet:1146)
Gordon syndrome (Orphanet:376)
NEMALINE MYOPATHY 5 (OMIM:605355)
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGERTYPE (OMIM:609223)
Spondyloepimetaphyseal dysplasia - hypotrichosis (Orphanet:168443)