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Diseases

Hip Dislocation, Congenital

hip dislocation, congenital

Entity Type
Diseases
Relation Groups
3
Relation Preview
24

Basic Information

Grouped by core information, identifiers, and descriptions.

Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.

Core Information

Disease Name
Hip Dislocation, Congenital
Standard Disease Name
hip dislocation, congenital
MeSH Tree
No data
ICD-10
Q65.2

Identifiers

DO ID
No data
MeSH ID
D006618
OMIM ID
MTHU001429|MTHU051514|MTHU012362|MTHU019061|MTHU017649|MTHU007218|142700
UMLS ID
C0019555
HPO ID
No data

Description and Extensions

Description
NCI2016_NICHD_1602D:A spectrum of hip abnormalities commonly presenting in infancy involving the relationship between the femoral head and the acetabulum and that includes subluxation or dislocation at rest or upon provocation.|NCI2016_02D:A spectrum of hip abnormalities commonly presenting in infancy involving the relationship between the femoral head and the acetabulum and that includes subluxation or dislocation at rest or upon provocation.|MSH2017_2016_08_12:Congenital dislocation of the hip generally includes subluxation of the femoral head, acetabular dysplasia, and complete dislocation of the femoral head from the true acetabulum. This condition occurs in approximately 1 in 1000 live births and is more common in females than in males.|HPO2016_07_04:The presence of developmental dysplasia of the hip. [HPO:probinson]
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
01
AKR1C1
aldo-keto reductase family 1 member C1
aldo-keto reductase family 1 member C1
02
ALDH18A1
aldehyde dehydrogenase 18 family member A1
aldehyde dehydrogenase 18 family member A1
07
GDF5
growth differentiation factor 5
growth differentiation factor 5