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Ontology Browser

Term:
Camptodactyly Joint Contractures and Facial Skeletal Dysplasia (DOID:9006103)
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Parent Terms Term With Siblings Child Terms
clubfoot +     
Contracture +     
dysostosis +     
Aarskog syndrome +   
Aase Smith Syndrome 
Achard syndrome 
acheiropody  
acrodysostosis +   
acrofacial dysostosis +   
acrofacial dysostosis Rodriguez type 
acrofacial dysostosis, Patagonia type 
acrofrontofacionasal dysostosis 
acromelic frontonasal dysostosis  
Acrootoocular Syndrome 
acrorenal syndrome +  
Agenesis of Cervical Vertebrae 
Alopecia Contractures Dwarfism Mental Retardation 
Anonychia-Ectrodactyly 
Anonychia-Onychodystrophy with Hypoplasia or Absence of Distal Phalanges 
Axial Mesodermal Dysplasia Spectrum 
Banki Syndrome 
Bethlem myopathy +   
Bone Fragility with Contractures, Arterial Rupture, and Deafness  
Bowen Syndrome 
brachydactyly +   
brachydactyly type E1  
brachydactyly type E2  
Camptodactyly 1 
Camptodactyly Joint Contractures and Facial Skeletal Dysplasia 
Camptodactyly Syndrome Guadalajara Type 1 
Camptodactyly Syndrome Guadalajara Type 2 
Camptodactyly Taurinuria 
Camptodactyly Vertebral Fusion 
Camptodactyly, Fibrous Tissue Hyperplasia, and Skeletal Dysplasia 
camptodactyly-arthropathy-coxa vara-pericarditis syndrome  
Camptodactyly-Ichthyosis Syndrome 
camptodactyly-tall stature-scoliosis-hearing loss syndrome  
Camptosynpolydactyly, Complex  
Carnevale Hernandez Castillo Syndrome 
Catel Manzke Syndrome  
Cenani-Lenz syndactyly syndrome  
Chitayat Meunier Hodgkinson Syndrome 
Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly 
Coffin-Siris syndrome +   
cold-induced sweating syndrome +   
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 
Cousin Syndrome  
Crane-Heise Syndrome 
Cranioacrofacial Syndrome 
Craniosynostosis, Adelaide Type 
Crouzon syndrome +   
Daneman Davy Mancer Syndrome 
Davenport Donlan Syndrome 
Deafness, Congenital Onychodystrophy, Recessive Form 
Diaphanospondylodysostosis  
Digitorenocerebral Syndrome  
Digitotalar Dysmorphism 
Distal Symphalangism +   
Dupuytren Contracture +  
Dwarfism Stiff Joint Ocular Abnormalities 
Dystelephalangy 
Dystonia with Ringbinden 
Ectodermal Dysplasia, Ectrodactyly, and Macular Dystrophy  
Ectrodactyly and Ectodermal Dysplasia without Cleft Lip/Palate 
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1 
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3  
Ectrodactyly-Cleft Palate Syndrome 
Ehlers-Danlos Syndrome, Musculocontractural Type 2  
Eiken Skeletal Dysplasia  
Erosive Arthropathy 
Extensor Tendons of Fingers, Anomalous Insertion of 
Facial Dysmorphism, Cleft Palate, Hearing Loss, and Camptodactyly 
Fairbank Disease 
Femur Bifid with Monodactylous Ectrodactyly 
Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome 
focal dermal hypoplasia +   
Frints De Smet Fabry Fryns Syndrome 
Fronto-Facio-Nasal Dysplasia 
Frontonasal Dysplasia 1  
Frontootopalatodigital Osteodysplasia 
Fuhrmann syndrome  
Gingival Fibromatosis with Hypertrichosis and Mental Retardation 
Goodman Camptodactyly 
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 
Growth Mental Deficiency Syndrome of Myhre  
Growth Retardation, Small and Puffy Hands and Feet, and Eczema 
Hairy Palms and Soles 
hand-foot-genital syndrome  
Heart-Hand Syndrome, Slovenian Type  
Hecht Scott Syndrome 
Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis  
hereditary spastic paraplegia 18  
Hip Contracture 
Histiocytosis with Joint Contractures and Sensorineural Deafness  
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate  
hydrolethalus syndrome +   
Iida Kannari Syndrome 
Inclusion Body Myopathy 3, Autosomal Dominant  
Isolated Thoracic Dysostosis 
Johnson Munson Syndrome 
Keutel Syndrome  
Khalifa Graham Syndrome 
Klippel-Feil syndrome +   
Lambert Syndrome 
Laurin-Sandrow Syndrome  
Leri Pleonosteosis 
lethal congenital contracture syndrome 3  
lethal restrictive dermopathy  
Macleod Fraser syndrome 
Macrodactyly of the Hand 
Mammary-Digital-Nail Syndrome 
Mandibulofacial Dysostosis Syndrome, Bauru Type 
Mandibulofacial Dysostosis with Macroblepharon and Macrostomia 
Marden Walker Like Syndrome  
Marden-Walker Syndrome  
Mental Retardation Mietens Weber Type 
Mental Retardation, Microcephaly, Growth Retardation, Joint Contractures, and Facial Dysmorphism 
Metacarpal 4 5 Fusion  
Metaphyseal Acroscyphodysplasia 
Metaphyseal Dysostosis, Mental Retardation, and Conductive Deafness 
Michels Caskey Syndrome 
Microcephaly with Mental Retardation and Digital Anomalies  
Miles-Carpenter syndrome  
Mononen-Karnes-Senac syndrome 
Morillo-Cucci Passarge Syndrome 
Muller Barth Menger Syndrome 
Multiple Pterygium Syndrome, X-Linked 
Neurofaciodigitorenal Syndrome 
Oculootoradial Syndrome  
Odontotrichoungual-Digital-Palmar Syndrome 
Oroacral Syndrome, Verloes-Koulischer Type 
orofaciodigital syndrome +   
Oslam syndrome 
Oto-Palato-Digital Syndrome Type 1  
Oto-Palato-Digital Syndrome, Type 2  
Otopalatodigital Spectrum Disorder  
Partial Aphalangia with Syndactyly and Duplication of Metatarsal IV 
Patent Ductus Arteriosus and Bicuspid Aortic Valve with Hand Anomalies 
Pfeiffer Tietze Welte Syndrome 
plantar fascial fibromatosis 
Postaxial Polydactyly, with Dental and Vertebral Anomalies 
Progeroid Facial Appearance with Hand Anomalies 
Pseudotrisomy 13 Syndrome 
Radio-Ulnar Synostosis Type 1 
Radio-Ulnar Synostosis Type 2 
Rhizomelic Dysplasia Patterson Lowry Type 
Richieri Costa Guion-Almeida Syndrome 
Richieri Costa Pereira Syndrome  
Rozin Hertz Goodman Syndrome 
Rubinstein-Taybi syndrome +   
Saal Bulas Syndrome 
Sanderson Fraser Syndrome 
Santos Syndrome 
Say Field Coldwell syndrome 
Schinzel-Giedion Syndrome  
Second Metatarsal-Metacarpal Syndrome 
Split Hand Split Foot Nystagmus 
split hand-foot malformation 1 with sensorineural hearing loss  
Spondylocamptodactyly 
spondylocostal dysostosis +   
Spondylospinal Thoracic Dysostosis 
Stiff Skin Syndrome  
Stoll Alembik Dott Syndrome 
Symphalangism with Multiple Anomalies of Hands and Feet 
Symphalangism, C. S. Lewis Type 
synostosis +   
Synostosis, Carpal, with Dysplastic Elbow Joints and Brachydactyly  
Synpolydactyly 2  
Tabatznik Syndrome 
TARP Syndrome  
tarsal-carpal coalition syndrome  
Teebi Kaurah Syndrome 
Teebi Syndrome 
Tel Hashomer Camptodactyly Syndrome 
Terminal Osseous Dysplasia and Pigmentary Defects  
Thoracopelvic Dysostosis 
Tollner Horst Manzke Syndrome 
trichorhinophalangeal syndrome type III  
Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet 
Triphalangeal Thumb +   
Tukel Syndrome 
Ulnar Hypoplasia with Mental Retardation 
Unilateral Adactylia 
Unilateral Aplasia of Extensor Muscles of Fingers, with Generalized Polyneuropathy 
Van Maldergem syndrome +   
Ventricular Extrasystoles Perodactyly Robin Sequence 
Vohwinkel Syndrome  
Volkmann contracture 
Walbaum Titran Durieux Crepin Syndrome 
Weaver syndrome  
Weyers Ulnar Ray/Oligodactyly Syndrome 
Winchester Syndrome  
Winter Harding Hyde Syndrome 
X-linked Emery-Dreifuss muscular dystrophy 1  
Zimmerman Laband Syndrome  

Synonyms
Primary IDs: MESH:C537969 ;   RDO:0003897

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