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Congenital Contractures, Torticollis, and Malignant Hyperthermia (DOID:9001286)
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Parent Terms Term With Siblings Child Terms
cervical dystonia +     
Contracture +     
Aase Smith Syndrome 
Alopecia Contractures Dwarfism Mental Retardation 
Axial Mesodermal Dysplasia Spectrum 
Bethlem myopathy +   
Bone Fragility with Contractures, Arterial Rupture, and Deafness  
Bowen Syndrome 
Calabro Syndrome 
Camptodactyly Joint Contractures and Facial Skeletal Dysplasia 
cleft lip +   
cleft palate +   
cleft palate-lateral synechia syndrome  
congenital contractural arachnodactyly  
Congenital Contractures, Torticollis, and Malignant Hyperthermia 
Congenital Ectodermal Dysplasia with Hearing Loss 
Congenital Torticollis 
Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndromes +   
Davenport Donlan Syndrome 
Dupuytren Contracture +  
Dystonia with Ringbinden 
Erosive Arthropathy 
gingival fibromatosis +   
Growth Deficiency and Mental Retardation with Facial Dysmorphism  
Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy 
Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis  
hereditary spastic paraplegia 18  
Hip Contracture  
histiocytosis-lymphadenopathy plus syndrome  
Iida Kannari Syndrome 
Jagell Holmgren Hofer Syndrome 
King Denborough Syndrome  
lethal congenital contracture syndrome 3  
lethal restrictive dermopathy  
Macleod Fraser syndrome 
Macrostomia +   
Malignant Fever  
Marden-Walker Syndrome  
Mental Retardation Mietens Weber Type 
Mental Retardation, Microcephaly, Growth Retardation, Joint Contractures, and Facial Dysmorphism 
Microstomia +  
Miles-Carpenter syndrome +   
multiple pterygium syndrome +   
Multiple Pterygium Syndrome, X-Linked 
Native American myopathy  
orofacial cleft +   
plantar fascial fibromatosis 
proximal myopathy and ophthalmoplegia  
Rozin Hertz Goodman Syndrome 
Sandifer Syndrome 
Spondylospinal Thoracic Dysostosis 
stiff skin syndrome  
Taurodontism, Microdontia, and Dens Invaginatus 
temtamy preaxial brachydactyly syndrome  
Torticollis Keloids Cryptorchidism Renal Dysplasia 
Van den Ende-Gupta syndrome  
Velopharyngeal Insufficiency 
Verloove-Vanhorick Brubakk Syndrome 
Volkmann contracture 
Warburg-Cinotti Syndrome  
Winchester syndrome  
Winter Harding Hyde Syndrome 
X-linked Emery-Dreifuss muscular dystrophy 1  

Primary IDs: MESH:C565679
Alternate IDs: OMIM:217150

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