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Ontology Browser

Arthrogryposis Multiplex Congenita 3, Myogenic Type (DOID:9000909)
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Parent Terms Term With Siblings Child Terms
Arthrogryposis Multiplex Congenita 3, Myogenic Type 
An autosomal recessive disorder characterized by decreased fetal movements, hypotonia, variable skeletal defects, including clubfoot and scoliosis, and delayed motor milestones with difficulty walking.

Exact Synonyms: AMC3 ;   AMCM ;   arthrogryposis multiplex congenita, myogenic type
Replaced By: DOID:0080979
Definition Sources: OMIM:618484

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