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Ontology Browser
Term:
arthrogryposis due to muscular dystrophy (DOID:0110631)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
ARC syndrome +   
Arthrogryposis and Ectodermal Dysplasia 
arthrogryposis due to muscular dystrophy  
A congenital muscular dystrophy characterized by nonprogressive myopathy resulting in an arthrogryposis syndrome. (DO)
Arthrogryposis Epileptic Seizures Migrational Brain Disorder 
Arthrogryposis Multiplex Congenita 3, Myogenic Type  
Arthrogryposis Multiplex Congenita 5  
Arthrogryposis Multiplex Congenita Whistling Face 
Arthrogryposis Multiplex with Deafness, Inguinal Hernias, and Early Death 
Arthrogryposis, Cleft Palate, Craniosynostosis, and Impaired Intellectual Development  
Arthrogryposis, Mental Retardation, and Seizures  
ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY  
Arthrogryposis, X-Linked, Type V 
Bethlem myopathy +   
Boylan Dew Greco Syndrome 
Bruck syndrome +   
Camptodactyly-Ichthyosis Syndrome 
CAP-Congenital Myopathy with Arthrogryposis Multiplex Congenita without Heart Involvement 
Cataract, Microcephaly, Arthrogryposis, Kyphosis Syndrome 
Cerebrooculofacioskeletal Syndrome 2  
Cerebrooculofacioskeletal Syndrome 4  
Congenital Arthrogryposis with Anterior Horn Cell Disease  
congenital merosin-deficient muscular dystrophy 1A +   
congenital muscular dystrophy 1B 
Congenital Muscular Dystrophy associated with Calf Hypertrophy, Microcephaly, and Severe Mental Retardation 
congenital muscular dystrophy due to integrin alpha-7 deficiency  
congenital muscular dystrophy due to LMNA mutation  
congenital muscular dystrophy merosin-positive 
Congenital Muscular Dystrophy plus Mental Retardation 
congenital muscular dystrophy with cataracts and intellectual disability  
Congenital Muscular Dystrophy with Cerebellar Atrophy 
Congenital Muscular Dystrophy with Rapid Progression 
Congenital Muscular Dystrophy with Severe Central Nervous System Atrophy and Absence of Large Myelinated Fibers 
Congenital Muscular Dystrophy, Davignon-Chauveau Type  
Congenital Neuropathy with Arthrogryposis Multiplex 
Cyprus Facial Neuromusculoskeletal Syndrome 
distal arthrogryposis +   
Ehlers-Danlos syndrome musculocontractural type 2  
fetal akinesia deformation sequence syndrome +   
German Syndrome 
hereditary neuropathy with liability to pressure palsies  
Holoprosencephaly with Fetal Akinesia/Hypokinesia Sequence 
Intellectual Disability with Episodic Ataxia and Congenital Arthrogryposis  
Jequier Kozlowski Skeletal Dysplasia 
Johnston Aarons Schelley Syndrome 
Ladda Zonana Ramer syndrome 
lethal congenital contracture syndrome +   
Massa Casaer Ceulemans Syndrome 
megaconial type congenital muscular dystrophy  
Minicore Myopathy, Antenatal Onset, with Arthrogryposis 
Multiple Pterygium Syndrome, Lethal Type  
muscular dystrophy-dystroglycanopathy +   
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ARTHROGRYPOSIS, AND STRUCTURAL BRAIN ANOMALIES  
neurogenic arthrogryposis multiplex congenita +   
Pelvic Dysplasia Arthrogryposis of Lower Limbs 
Podder-Tolmie Syndrome 
POLYMICROGYRIA, PERISYLVIAN, WITH CEREBELLAR HYPOPLASIA AND ARTHROGRYPOSIS  
Ray Peterson Scott Syndrome 
rigid spine muscular dystrophy 1  
Spondylohypoplasia, Arthrogryposis and Popliteal Pterygium 
Spranger Schinzel Myers Syndrome 
Ullrich congenital muscular dystrophy +   
Walker-Warburg syndrome +   

Synonyms
Exact Synonyms: congenital muscular dystrophy producing arthrogryposis ;   muscular dystrophy and arthrogryposis
Primary IDs: MESH:C564985
Alternate IDs: OMIM:253900
Xrefs: GARD:779 ;   ICD10CM:M62.8 ;   ORDO:1155
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/13942250 "DO"

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