Ontology Browser

Term:
tarsal-carpal coalition syndrome (DOID:0050789)
Annotations: Rat: (3) Mouse: (3) Human: (4) Chinchilla: (3) Bonobo: (3) Dog: (3) Squirrel: (3)
Parent Terms Term With Siblings Child Terms
ankylosis +     
hyperopia +     
syndactyly +     
synostosis +     
Aarskog syndrome +   
abdominal obesity-metabolic syndrome +   
ablepharon macrostomia syndrome  
acheiropody  
achondrogenesis type II  
acrocephalosyndactylia +   
acrofacial dysostosis Cincinnati type  
acrofacial dysostosis Rodriguez type 
acrofacial dysostosis, Patagonia type 
acrokeratosis verruciformis  
Acrootoocular Syndrome 
acrorenal syndrome +  
ADULT syndrome  
adult-onset autosomal dominant demyelinating leukodystrophy  
adult-onset leukoencephalopathy with axonal spheroids and pigmented glia  
advanced sleep phase syndrome +   
age related macular degeneration +   
Alexander Disease  
Alzheimer's disease 1 +   
Alzheimer's disease 2  
Alzheimer's disease 3 +   
Alzheimer's disease 4  
Alzheimer's disease 5 
amelogenesis imperfecta type 1A  
amelogenesis imperfecta type 1B  
amelogenesis imperfecta type 3A  
amelogenesis imperfecta type 3B  
amelogenesis imperfecta type 4  
Andersen-Tawil syndrome  
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome  
ankylosing spondylitis +   
Anonychia-Ectrodactyly 
Anonychia-Onychodystrophy with Hypoplasia or Absence of Distal Phalanges 
Antley-Bixler syndrome +   
Aphalangia Syndactyly Microcephaly 
APP-related cerebral amyloid angiopathy  
arrhythmogenic right ventricular dysplasia 1  
arrhythmogenic right ventricular dysplasia 10  
arrhythmogenic right ventricular dysplasia 11  
arrhythmogenic right ventricular dysplasia 12  
arrhythmogenic right ventricular dysplasia 13  
arrhythmogenic right ventricular dysplasia 2  
arrhythmogenic right ventricular dysplasia 3 
arrhythmogenic right ventricular dysplasia 4 
arrhythmogenic right ventricular dysplasia 5  
arrhythmogenic right ventricular dysplasia 8  
arrhythmogenic right ventricular dysplasia 9  
atrial heart septal defect 2  
atrial heart septal defect 5  
atrial heart septal defect 6  
atrial heart septal defect 7  
atrial heart septal defect 8  
atrial heart septal defect 9  
Auriculocondylar Syndrome +   
Aurocephalosyndactyly 
autoimmune lymphoproliferative syndrome type 2A  
autoimmune lymphoproliferative syndrome type 4  
autosomal dominant Alport syndrome  
autosomal dominant cerebellar ataxia +   
autosomal dominant chondrodysplasia punctata +  
autosomal dominant chronic granulomatous disease 
autosomal dominant cutis laxa +   
Autosomal Dominant Dyskeratosis Congenita +   
autosomal dominant Emery-Dreifuss muscular dystrophy 4  
autosomal dominant Emery-Dreifuss muscular dystrophy 5  
autosomal dominant Emery-Dreifuss muscular dystrophy 7  
autosomal dominant familial periodic fever  
autosomal dominant hypocalcemia +   
autosomal dominant hypophosphatemic rickets  
autosomal dominant isolated ectopia lentis 1  
autosomal dominant keratitis-ichthyosis-deafness syndrome  
autosomal dominant limb-girdle muscular dystrophy +   
autosomal dominant macrothrombocytopenia TUBB1-related  
autosomal dominant mental retardation 55  
autosomal dominant mental retardation 56  
autosomal dominant microcephaly +   
autosomal dominant nocturnal frontal lobe epilepsy +   
autosomal dominant non-syndromic intellectual disability +   
autosomal dominant nonsyndromic deafness +   
autosomal dominant osteopetrosis 1  
autosomal dominant osteopetrosis 2  
autosomal dominant Parkinson's disease 1  
autosomal dominant Parkinson's disease 22  
autosomal dominant Parkinson's disease 4  
autosomal dominant Parkinson's disease 8  
autosomal dominant polycystic kidney disease +   
autosomal dominant pseudohypoaldosteronism type 1  
autosomal dominant Robinow syndrome 1  
autosomal dominant Robinow syndrome 2  
autosomal dominant Robinow syndrome 3  
autosomal dominant sensory ataxia 1  
autosomal dominant sideroblastic anemia 4  
autosomal dominant type IV Ehlers-Danlos syndrome +   
Autosomal Recessive Syndrome of Syndactyly, Undescended Testes and Central Nervous System Defects  
Axenfeld-Rieger syndrome +   
Banki Syndrome 
Bannayan-Riley-Ruvalcaba syndrome  
Bart-Pumphrey syndrome  
Beare-Stevenson cutis gyrata syndrome  
Birk-Barel syndrome  
Birt-Hogg-Dube syndrome  
Blau syndrome  
blepharocheilodontic syndrome +   
Blepharophimosis with Ptosis, Syndactyly, and Short Stature 
blepharophimosis, ptosis, and epicanthus inversus syndrome  
blue color blindness  
Bonneau Syndrome 
brachydactyly type A1 +   
brachydactyly type A2  
brachydactyly type C  
brachydactyly type D  
brachydactyly type E1  
brachydactyly type E2  
brachydactyly-syndactyly syndrome  
Brachyphalangy, Polydactyly, and Tibial Aplasia/Hypoplasia 
branchiooculofacial syndrome  
branchiootorenal syndrome +   
Brooke-Spiegler syndrome  
Brown-Vialetto-Van Laere syndrome +   
Brugada syndrome 1  
Brugada syndrome 7  
Brugada syndrome 9  
bullous congenital ichthyosiform erythroderma  
CADASIL 1  
CADASIL 2  
calcaneonavicular coalition 
campomelic dysplasia +   
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  
CAPOS Syndrome  
Carnevale Hernandez Castillo Syndrome 
Carney complex +   
Catel Manzke Syndrome  
Cenani-Lenz syndactyly syndrome  
Charcot-Marie-Tooth disease dominant intermediate A 
Charcot-Marie-Tooth disease dominant intermediate B +   
Charcot-Marie-Tooth disease dominant intermediate C  
Charcot-Marie-Tooth disease dominant intermediate D  
Charcot-Marie-Tooth disease dominant intermediate E  
Charcot-Marie-Tooth disease dominant intermediate F  
Charcot-Marie-Tooth Disease, Foot Deformity of 
cherubism +   
Chitayat Meunier Hodgkinson Syndrome 
cleft lip-palate-ectodermal dysplasia syndrome  
Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly 
Cleft Palate, Deafness, and Oligodontia 
Clouston syndrome  
Coffin-Siris syndrome +   
cold-induced sweating syndrome +   
Congenital Microtia +   
Cornelia de Lange syndrome 1  
Cornelia de Lange syndrome 3  
Cornelia de Lange syndrome 4  
Coronal Synostosis, Syndactyly and Jejunal Atresia 
Costello syndrome  
Cowden syndrome +   
Cranioacrofacial Syndrome 
craniosynostosis +   
Craniosynostosis, Adelaide Type 
Crossed Polysyndactyly 
Crouzon syndrome-acanthosis nigricans syndrome  
Culler-Jones syndrome  
Daneman Davy Mancer Syndrome 
Deafness, Congenital Onychodystrophy, Recessive Form 
Denys-Drash syndrome  
Der Kaloustian Mcintosh Silver Syndrome 
Digitorenocerebral Syndrome  
Digitotalar Dysmorphism 
discharging ear 
Distal Symphalangism +   
Duane-radial ray syndrome  
Duplication of Eyebrows with Stretchable Skin and Syndactyly 
Dwarfism Stiff Joint Ocular Abnormalities 
dysplastic nevus syndrome +   
Dystelephalangy 
Ear Deformities, Acquired 
Ear Neoplasms +  
Earache 
Ectodermal Dysplasia Mental Retardation Syndactyly 
Ectodermal Dysplasia, Ectrodactyly, and Macular Dystrophy  
Ectodermal Dysplasia-Syndactyly Syndrome +   
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 
EEC syndrome +   
Eiken Skeletal Dysplasia  
epidermolysis bullosa simplex generalized type  
epidermolysis bullosa simplex localized type  
Euhidrotic Ectodermal Dysplasia 
Extensor Tendons of Fingers, Anomalous Insertion of 
external ear disease +   
Facial Dysmorphism, Cleft Palate, Hearing Loss, and Camptodactyly 
Fairbank Disease 
familial cold autoinflammatory syndrome 4  
familial erythrocytosis 1  
familial erythrocytosis 3  
familial erythrocytosis 5  
Feingold syndrome +   
Femur Bifid with Monodactylous Ectrodactyly 
Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome 
Filippi Syndrome  
Fraser syndrome +   
Frasier syndrome  
Frias Syndrome 
Fried Goldberg Mundel Syndrome 
Frints De Smet Fabry Fryns Syndrome 
Frontootopalatodigital Osteodysplasia 
Fuhrmann syndrome  
Game Friedman Paradice Syndrome 
geniculate herpes zoster 
Gingival Fibromatosis with Hypertrichosis and Mental Retardation 
Gollop Coates Syndrome 
Goodman Camptodactyly 
Gordon Syndrome  
Grange Syndrome  
Green Sandford Davison Syndrome 
Growth Mental Deficiency Syndrome of Myhre  
Growth Retardation, Small and Puffy Hands and Feet, and Eczema 
Hairy Palms and Soles 
Hajdu-Cheney syndrome  
hand-foot-genital syndrome  
Hearing Disorders +   
Heart-Hand Syndrome, Slovenian Type  
Hecht Scott Syndrome 
hereditary breast ovarian cancer syndrome  
hereditary hemorrhagic telangiectasia +   
hereditary spastic paraplegia 10  
hereditary spastic paraplegia 12  
hereditary spastic paraplegia 13  
hereditary spastic paraplegia 19 
hereditary spastic paraplegia 29 
hereditary spastic paraplegia 31  
hereditary spastic paraplegia 33  
hereditary spastic paraplegia 36 
hereditary spastic paraplegia 37 
hereditary spastic paraplegia 38 
hereditary spastic paraplegia 3A  
hereditary spastic paraplegia 4  
hereditary spastic paraplegia 41 
hereditary spastic paraplegia 42  
hereditary spastic paraplegia 6  
hereditary spastic paraplegia 73  
hereditary spastic paraplegia 8  
high hyperopia  
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate  
Holt-Oram syndrome  
Humeroradial Multiple Synostosis Syndrome 
humeroradial synostosis 
Humeroradial Synostosis with Craniofacial Anomalies 
hydrolethalus syndrome +   
HYPERTELORISM, PREAURICULAR SINUS, PUNCTAL PITS, AND DEAFNESS 
hypomyelinating leukodystrophy 6  
hypophosphatasia +   
ichthyosis vulgaris +   
IMMUNODEFICIENCY 31C  
inner ear disease +   
iridogoniodysgenesis syndrome +   
Ischiopatellar Dysplasia  
Jackson-Weiss Syndrome  
Johnson Munson Syndrome 
Jorgenson Lenz Syndrome 
juvenile glaucoma  
juvenile polyposis syndrome +   
Keutel Syndrome  
Khalifa Graham Syndrome 
Kleiner Holmes Syndrome 
Kozlowski-Krajewska Syndrome 
Lachiewicz Sibley Syndrome 
LADD syndrome  
Landy Donnai Syndrome 
Larsen syndrome  
Laurin-Sandrow Syndrome  
LEOPARD syndrome +   
Leri Pleonosteosis 
Li-Fraumeni syndrome +   
Loeys-Dietz syndrome +   
Lynch syndrome +   
macrocephaly-autism syndrome  
Macrodactyly of the Foot 
Macrodactyly of the Hand 
malignant hyperthermia +   
Mammary-Digital-Nail Syndrome 
mandibulofacial dysostosis, Guion-Almeida type  
Martinez Monasterio Pinheiro Syndrome 
maturity-onset diabetes of the young +   
Meier-Gorlin syndrome 6  
Mesomelia-Synostoses Syndrome 
Metacarpal 4 5 Fusion  
Metaphyseal Acroscyphodysplasia 
Metatarsus Varus, Type I 
Michels Caskey Syndrome 
Microcephaly with Mental Retardation and Digital Anomalies  
Microcephaly, Microphthalmia, Ectrodactyly of Lower Limbs, and Prognathism  
Microphthalmia with Hyperopia, Retinal Degeneration, Macrophakia, and Dental Anomalies 
middle ear disease +   
mitochondrial DNA depletion syndrome 12a  
monilethrix +   
Mononen-Karnes-Senac syndrome 
Monophalangy of Great Toe 
Morillo-Cucci Passarge Syndrome 
Muckle-Wells syndrome  
Muller Barth Menger Syndrome 
multiple cutaneous and mucosal venous malformations  
Multiple Endocrine Neoplasia +   
multiple synostoses syndrome +   
myofibrillar myopathy 1  
myofibrillar myopathy 2  
myofibrillar myopathy 4  
myofibrillar myopathy 5  
myofibrillar myopathy 6  
Naguib-Richieri-Costa Syndrome 
nail-patella syndrome +   
Nanophthalmos 1 
Nanophthalmos 4  
necrosis of ear ossicle 
Neurofaciodigitorenal Syndrome 
neurofibromatosis +   
nevoid basal cell carcinoma syndrome +   
Nicolaides Baraitser Syndrome  
ocular albinism with sensorineural deafness  
oculodentodigital dysplasia +   
Oculodentodigital Dysplasia, Autosomal Recessive  
Oculodentoosseous Dysplasia Recessive 
Oculootoradial Syndrome  
Odontotrichoungual-Digital-Palmar Syndrome 
Opitz GBBB Syndrome, Type II  
Oroacral Syndrome, Verloes-Koulischer Type 
orofacial cleft 7 +   
Orstavik Lindemann Solberg Syndrome  
Oslam syndrome 
Otitis +   
Oto-Palato-Digital Syndrome Type 1  
Oto-Palato-Digital Syndrome, Type 2  
Otopalatodigital Spectrum Disorder  
otosclerosis +   
ovarian dysgenesis 8  
pachyonychia congenita +   
Pallister-Hall syndrome +   
PAPA syndrome  
paraganglioma +   
Partial Aphalangia with Syndactyly and Duplication of Metatarsal IV 
Patent Ductus Arteriosus and Bicuspid Aortic Valve with Hand Anomalies 
Pavone Fiumara Rizzo Syndrome 
Pelger-Huet anomaly +   
Periventricular Nodular Heterotopia with Syndactyly, Cleft Palate and Developmental Delay  
permanent neonatal diabetes mellitus +   
Pfeiffer Rockelein Syndrome 
Pfeiffer Tietze Welte Syndrome 
photosensitive trichothiodystrophy +   
piebaldism +   
Piepkorn Karp Hickok syndrome 
Piussan Lenaerts Mathieu syndrome 
Poland syndrome 
polycystic liver disease +   
popliteal pterygium syndrome +   
Postaxial Polydactyly, Type A4 
Postaxial Polydactyly, with Dental and Vertebral Anomalies 
Prata Libéral Gonçalves Syndrome 
Preauricular Tag, Isolated, Autosomal Dominant, 1 
Primrose Syndrome  
Progeroid Facial Appearance with Hand Anomalies 
proximal symphalangism  
Pseudoarthrogryposis 
Pseudotrisomy 13 Syndrome 
punctate palmoplantar keratoderma type III 
Question Mark Ears, Isolated  
Radial Defect Robin Sequence 
Radio-Ulnar Synostosis Type 1 
Radio-Ulnar Synostosis Type 2 
radioulnar synostosis  
Radioulnar Synostosis Retinal Pigment Abnormalities 
Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia +   
Radioulnar Synostosis, Radial Ray Abnormalities, and Severe Malformations in the Male 
Rapp-Hodgkin syndrome  
Ray Peterson Scott Syndrome 
renal coloboma syndrome  
retrocochlear disease +   
Rhizomelic Dysplasia Patterson Lowry Type 
Richieri Costa Guion-Almeida Syndrome 
Richieri Costa Pereira Syndrome  
Rosselli-Gulienetti Syndrome 
Rozin Hertz Goodman Syndrome 
Rubinstein-Taybi syndrome +   
Saal Bulas Syndrome 
SADDAN  
Sanderson Fraser Syndrome 
Sandhaus Ben-Ami Syndrome 
Say Field Coldwell syndrome 
Schinzel-Giedion Syndrome  
sclerosteosis +   
Second Metatarsal-Metacarpal Syndrome 
Short Stature, Facial Dysmorphism, Severe Brachydactyly, and Syndactyly 
Split Hand Split Foot Nystagmus 
split hand-foot malformation 1 with sensorineural hearing loss  
Spondylocamptodactyly 
spondylocarpotarsal synostosis syndrome  
spondyloepimetaphyseal dysplasia, Missouri type  
spondyloepimetaphyseal dysplasia, Strudwick type  
spondyloepiphyseal dysplasia congenita  
Stickler syndrome +   
Stoll Alembik Dott Syndrome 
strabismus +   
Supernumerary Der(22)t(8 
Susac Syndrome 
Symphalangism of Toes 
Symphalangism with Multiple Anomalies of Hands and Feet 
Symphalangism, C. S. Lewis Type 
syndactyly +   
Syndactyly, Mesoaxial Synostotic, with Phalangeal Reduction  
Syndactyly, Type 3  
Syndactyly, Type I  
Syndactyly, Type IV  
Syndactyly, Type V  
Syndactyly-Polydactyly-Earlobe Syndrome 
Synostosis of Talus and Calcaneus with Short Stature 
Synostosis, Carpal, with Dysplastic Elbow Joints and Brachydactyly  
synpolydactyly +   
Synpolydactyly 2  
Synpolydactyly with Foot Anomalies  
Tabatznik Syndrome 
Talipes +   
Talonavicular Coalition 
Tarsal Coalition 
tarsal-carpal coalition syndrome  
An autosomal dominant disease that is characterized by fusion of the carpals, tarsals, and phalanges, short first metacarpals causing brachydactyly; and humeroradial fusion. (DO)
Teebi Kaurah Syndrome 
Teebi Syndrome 
Tel Hashomer Camptodactyly Syndrome 
Temporomandibular Ankylosis 
Terminal Osseous Dysplasia and Pigmentary Defects  
Tietz syndrome  
Timothy syndrome  
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations  
Tollner Horst Manzke Syndrome 
tooth ankylosis +  
Townes-Brocks syndrome +   
transthyretin amyloidosis  
Treacher Collins syndrome +   
trichorhinophalangeal syndrome type I  
trichorhinophalangeal syndrome type II  
trichorhinophalangeal syndrome type III  
Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet 
Triphalangeal Thumb +   
Trueb Burg Bottani Syndrome 
Tsukahara Syndrome 
tuberous sclerosis +   
Tukel Syndrome 
Tympanic Membrane Perforation  
tympanosclerosis  
type 1 diabetes mellitus 2  
Ulnar Hypoplasia Lobster Claw Deformity of Feet 
Unilateral Adactylia 
Unilateral Aplasia of Extensor Muscles of Fingers, with Generalized Polyneuropathy 
Unilateral Radioulnar Synostosis with Developmental Retardation and Hypotonia 
Van Maldergem syndrome +   
Ventricular Extrasystoles Perodactyly Robin Sequence 
Vertical Talus, Congenital  
Vohwinkel Syndrome  
Waardenburg's syndrome +   
Walbaum Titran Durieux Crepin Syndrome 
Weaver syndrome  
Weyers Ulnar Ray/Oligodactyly Syndrome 
Winter Shortland Temple Syndrome  
Zechi-Ceide Syndrome 
Zerres Rietschel Majewski Syndrome 
Zimmerman Laband Syndrome  
Zygodactyly 1 

Synonyms
Exact Synonyms: STAPES ANKYLOSIS WITH BROAD THUMB AND TOES ;   Stapes Ankylosis Syndrome Without Symphalangism ;   TCC ;   Teunissen-Cremers syndrome ;   ankylosis of stapes, hyperopia, broad thumbs, broad first toes, and syndactyly ;   facioaudiosymphalangism syndrome ;   multiple synostoses syndrome 1 ;   multiple synostoses with brachydactyly ;   symphalangism-brachydactyly syndrome
Narrow Synonyms: synostosis of talus and calcaneus with short stature
Primary IDs: MESH:C536943
Alternate IDs: OMIM:184460 ;   OMIM:186570 ;   RDO:0002671 ;   RDO:0008164
Definition Sources: http://ghr.nlm.nih.gov/condition/tarsal-carpal-coalition-syndrome, http://omim.org/entry/186570?search=186570&highlight=186570, http://rarediseases.info.nih.gov/gard/9225/tarsal-carpal-coalition-syndrome/resources/1, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1412, https://www.ncbi.nlm.nih.gov/pubmed/22326510

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