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Ontology Browser

Term:
Distal Arthrogryposis Multiplex Congenita, Type 1 (DOID:9006007)
Annotations: Rat: (6) Mouse: (7) Human: (7) Chinchilla: (5) Bonobo: (6) Dog: (6) Squirrel: (6) Pig: (6)
Parent Terms Term With Siblings Child Terms
Arthrogryposis-like Hand Anomaly and Sensorineural Deafness 
Congenital Contractural Arachnodactyly  
Distal Arthrogryposis Multiplex Congenita, Type 1 +   
Distal Arthrogryposis Multiplex Congenita, X-Linked  
Distal Arthrogryposis, Moore Weaver Type 
Distal Arthrogryposis, Type 10 
Distal Arthrogryposis, Type 2 +   
Distal Arthrogryposis, Type 4 
Distal Arthrogryposis, Type 5D  
Distal Arthrogryposis, with Hypopituitarism, Mental Retardation, and Facial Anomalies 
Distal Arthrogryposis, with Impaired Proprioception and Touch  
Distal Arthrogryposis, with Mental Retardation and Characteristic Facies 
Freeman-Sheldon Syndrome  
Gordon Syndrome  
Hecht Syndrome  
Oculomelic Amyoplasia  

Synonyms
Exact Synonyms: AMCD1 ;   DA1 ;   distal arthrogryposis multiplex congenita, type I ;   distal arthrogryposis type 1
Primary IDs: MESH:C535378
Alternate IDs: RDO:0000467

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