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Ontology Browser

Term:
Congenital Contractural Arachnodactyly (DOID:9006681)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
Arachnodactyly +     
Contracture +     
Aase Smith Syndrome 
Achard syndrome 
Alopecia Contractures Dwarfism Mental Retardation 
Arachnodactyly Ataxia Cataract Aminoaciduria Mental Retardation 
Arthrogryposis-like Hand Anomaly and Sensorineural Deafness 
Axial Mesodermal Dysplasia Spectrum 
Bethlem myopathy +   
Bhaskar Jagannathan Syndrome 
Bone Fragility with Contractures, Arterial Rupture, and Deafness  
Bowen Syndrome 
Camptodactyly Joint Contractures and Facial Skeletal Dysplasia 
Congenital Contractural Arachnodactyly  
CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY  
Congenital Contractures, Torticollis, and Malignant Hyperthermia 
Congenital Ectodermal Dysplasia with Hearing Loss 
Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1A  
Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1B  
Davenport Donlan Syndrome 
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 
Dupuytren Contracture +  
Dystonia with Ringbinden 
Erosive Arthropathy 
Freeman-Sheldon Syndrome  
Gordon Syndrome  
Growth Deficiency and Mental Retardation with Facial Dysmorphism  
Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy 
Hecht Syndrome  
Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis  
hereditary spastic paraplegia 18  
Hip Contracture 
histiocytosis-lymphadenopathy plus syndrome  
Iida Kannari Syndrome 
Inclusion Body Myopathy 3, Autosomal Dominant  
Jaffer Beighton Syndrome 
Kosztolanyi Syndrome 
lethal congenital contracture syndrome 3  
lethal restrictive dermopathy  
Macleod Fraser syndrome 
Marden Walker Like Syndrome  
Marden-Walker Syndrome  
Mental Retardation Mietens Weber Type 
Mental Retardation, Microcephaly, Growth Retardation, Joint Contractures, and Facial Dysmorphism 
Miles-Carpenter syndrome  
Multiple Pterygium Syndrome, X-Linked 
Oculomelic Amyoplasia  
plantar fascial fibromatosis 
Rozin Hertz Goodman Syndrome 
Scoliosis, Arachnodactyly, and Blindness 
Shprintzen Golberg Craniosynostosis  
Spondylospinal Thoracic Dysostosis 
Stiff Skin Syndrome  
Volkmann contracture 
Winchester Syndrome  
Winter Harding Hyde Syndrome 
X-linked Emery-Dreifuss muscular dystrophy 1  

Synonyms
Exact Synonyms: Arachnodactyly, contractural Beals type ;   Arthrogryposis, Distal, Type 9 ;   Beals syndrome ;   Beals-Hecht syndrome ;   CCA ;   Contractures, multiple with arachnodactyly ;   DA9 ;   Ear anomalies-contractures-dysplasia of bone with kyphoscoliosis
Primary IDs: MESH:C536211 ;   RDO:0001692
Alternate IDs: OMIM:121050

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