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Ontology Browser

Term:
CAP-Congenital Myopathy with Arthrogryposis Multiplex Congenita without Heart Involvement (DOID:9004836)
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Parent Terms Term With Siblings Child Terms
Arthrogryposis +     
Cap Myopathy +    
ARC syndrome +   
Arthrogryposis and Ectodermal Dysplasia 
arthrogryposis due to muscular dystrophy  
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 
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 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 
Minicore Myopathy, Antenatal Onset, with Arthrogryposis 
Multiple Pterygium Syndrome, Lethal Type  
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 
Spondylohypoplasia, Arthrogryposis and Popliteal Pterygium 
Spranger Schinzel Myers Syndrome 

Synonyms
Primary IDs: RDO:9000398

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.