Arthrogryposis, congenital, lower limb, X-linked

Preferred Label : Arthrogryposis, congenital, lower limb, X-linked;

Symbol : ACLLX;

CISMeF acronym : ACLLX; AMCX5;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Arthrogryposis, X-linked, type V; AMCX5;

Inheritance : X-linked recessive;

Prefixed ID : %300158;

Details

Origin ID

300158;

UMLS CUI

C1846273;

Automatic exact mappings (from CISMeF team)
- arthrogryposis, X-Linked, type V [MeSH concept]
- arthrogryposis, X-Linked, type V [MeSH Supplementary Concept]
HPO term(s)
- Ankle flexion contracture [HPO term]
- Arthrogryposis multiplex congenita [HPO term]
- Gait disturbance [HPO term]
- Hip contracture [HPO term]
- Knee flexion contracture [HPO term]
- Nonprogressive [HPO term]
- Pes planus [HPO term]
- X-linked inheritance [HPO term]
- X-linked recessive inheritance [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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