Dislocation of hip, congenital, with hyperextensibility of fingers and facial dysmorphism

Preferred Label : Dislocation of hip, congenital, with hyperextensibility of fingers and facial dysmorphism;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Hip, congenital dislocation of, with hyperextensibility of fingers and facial dysmorphism;

Inheritance : Autosomal dominant;

Prefixed ID : 601450;

Details

Origin ID

601450;

UMLS CUI

C1832353;

Automatic exact mappings (from CISMeF team)
- dislocation of hip, congenital, with hyperextensibility of fingers and facial dysmorphism [MeSH concept]
Currated CISMeF NLP mapping
- Dislocation of hip and facial dysmorphism syndrome (disorder) [SNOMED CT concept]
- Dislocation of the hip-dysmorphism syndrome [ORDO Disease]
- dislocation of hip, congenital, with hyperextensibility of fingers and facial dysmorphism [MeSH Supplementary Concept]
HPO term(s)
- Atrial septal defect [HPO term]
- Autosomal dominant inheritance [HPO term]
- Congenital hip dislocation [HPO term]
- Congenital knee dislocation [HPO term]
- Epicanthus [HPO term]
- Flat face [HPO term]
- Hypertelorism [HPO term]
- Inguinal hernia [HPO term]
- Joint hypermobility [HPO term]
- Joint laxity [HPO term]
- Joint laxity, mild [HPO term]
- Malar flattening [HPO term]
- Mild short stature [HPO term]
- Patent ductus arteriosus [HPO term]
- Patent foramen ovale [HPO term]
- Relative short stature [HPO term]
- Vesicoureteral reflux [HPO term]
- Wide nasal bridge [HPO term]
ORDO concept(s)
- Dislocation of the hip-dysmorphism syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Dislocation of the hip-dysmorphism syndrome [ORDO Disease]
- dislocation of hip, congenital, with hyperextensibility of fingers and facial dysmorphism [MeSH Supplementary Concept]
- dislocation of hip, congenital, with hyperextensibility of fingers and facial dysmorphism [MeSH concept]

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