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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Talipes +     
Acro-Osteolysis +   
Agonadism, XY, with Mental Retardation, Short Stature, Retarded Bone Age, and Multiple Extragenital Malformations 
Angel Shaped Phalangoepiphyseal Dysplasia 
Au-Kline Syndrome  
Baby Rattle Pelvis Dysplasia 
Battaglia Neri Syndrome 
Bazopoulou Kyrkanidou Syndrome 
Bellini Chiumello Rimoldi Syndrome 
Bent Bone Dysplasia Syndrome  
Blount's disease 
Bone Dysplasia, Lethal, Holmgren Type 
Brachioskeletogenital Syndrome  
Brachymesomelia Renal Syndrome 
Brittle Bone Disorder 
Camptodactyly, Fibrous Tissue Hyperplasia, and Skeletal Dysplasia 
camptodactyly-tall stature-scoliosis-hearing loss syndrome  
Cervical Vertebral Dysplasia 
CHOPS SYNDROME  
clubfoot +   
A deformed foot in which the foot is plantarflexed, inverted, and adducted.
Cortical Defects, Wormian Bones, and Dentinogenesis Imperfecta 
craniolenticulosutural dysplasia  
Deafness Conductive Ptosis Skeletal Anomalies 
Diaphragmatic Defects, Limb Deficiencies, and Ossification Defects Of Skull 
Diaphyseal Medullary Stenosis with Malignant Fibrous Histiocytoma  
Doughnut Lesions of Skull, Familial  
Dwarfism +   
dysostosis +   
Dysplasia Epiphysealis Hemimelica +  
Equinus Deformity 
EVEN-PLUS SYNDROME  
Flatfoot  
Fountain Syndrome 
Fryns Hofkens Fabry Syndrome 
Fuhrmann syndrome  
Funnel Chest +   
Gigantism +   
Gorham's disease +  
Gracile Bone Dysplasia  
Gurrieri Sammito Bellussi Syndrome 
Hall Riggs Mental Retardation Syndrome 
Kantaputra Gorlin Syndrome 
KBG syndrome  
Kozlowski Rafinski Klicharska Syndrome 
Kozlowski Warren Fisher Syndrome 
Kyphomelic Dysplasia 
Leg Length Inequality 
Lenz-Majewski hyperostotic dwarfism  
Lissencephaly Type III and Bone Dysplasia 
Macroepiphyseal Dysplasia, McAlister Coe Type 
Marfan syndrome +   
Marshall-Smith syndrome  
Membranous Cranial Ossification, Delayed 
Mesomelic Dysplasia, Camera Type 
Mesomelic Limb Shortening and Bowing 
Miura type epiphyseal chondrodysplasia  
nevoid basal cell carcinoma syndrome +   
osteochondrodysplasia +   
Osteofibrous Dysplasia  
Osteosclerosis with Ichthyosis and Premature Ovarian Failure 
Patterson Pseudoleprechaunism Syndrome 
Pectus Carinatum  
Platybasia +  
Pointer Syndrome 
Prenatal Bowing 
Proteus syndrome +   
Radius Absent Anogenital Anomalies 
Rhizomelic Dysplasia Patterson Lowry Type 
Rhizomelic Dysplasia, Scoliosis, and Retinitis Pigmentosa 
Rhizomelic Skeletal Dysplasia with Retinitis Pigmentosa 
Rhizomelic Syndrome 
Roifman-Chitayat Syndrome 
Santos Syndrome 
Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, Skeletal Abnormalities  
SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES  
SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES  
Shwachman-Diamond Syndrome 2  
Skeletal Defects, Genital Hypoplasia, And Mental Retardation  
Skeletal Dysplasia And Progressive Central Nervous System Degeneration, Lethal 
Skeletal Dysplasia with Delayed Epiphyseal and Carpal Bone Ossification 
split hand-foot malformation +   
Spondyloepimetaphyseal Dysplasia, Aggrecan Type  
Spranger Schinzel Myers Syndrome 
Stoll Levy Francfort Syndrome 
Talipes Cavus  
Trichoodontoonychial Dysplasia 
Ulnar Hypoplasia with Mental Retardation 
Verheij Syndrome  
Vertebral Body Fusion Overgrowth 
Weismann Netter Syndrome 
Wiedemann Oldigs Oppermann Syndrome 

Synonyms
Exact Synonyms: CCF ;   Congenital Clubfeet ;   Congenital Clubfoot ;   Congenital Talipes Equinovarus ;   Congenital equinovarus ;   Equinovarus ;   Equinovarus deformity of foot ;   Idiopathic congenital talipes equinovarus ;   Pie Torcido ;   Pie Torcidos ;   clubfeet ;   congenital clubfoot with or without deficiency of long bones and/or mirror-image polydactyly ;   talipes equinovarus
Narrow Synonyms: BILATERAL TALIPES EQUINOVARUS
Primary IDs: MESH:D003025
Alternate IDs: OMIM:119800
Xrefs: ICD10CM:Q66.0 ;   ICD10CM:Q66.89 ;   ICD9CM:754.51 ;   NCI:C84641
Definition Sources: MESH:D003025, http://en.wikipedia.org/wiki/Club_foot, https://www.ncbi.nlm.nih.gov/pubmed/17610748

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