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Pathways
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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Congenital Hand Deformities +   
Alterations or deviations from normal shape or size which result in a disfigurement of the hand occurring at or before birth.
Cubitus Valgus with Impaired Intellectual Development and Unusual Facies 
Fryns Hofkens Fabry Syndrome 
Hand Deformities, Acquired 
Holt-Oram syndrome  
Hypomelia Mullerian Duct Anomalies 
Ophthalmomandibulomelic Dysplasia 
Radio Renal Syndrome 
Tamari Goodman Syndrome 
Terminal Transverse Defects of Arm 
thrombocytopenia-absent radius syndrome  
Thumb Deformity +   
Ulnar Hypoplasia with Lobster-Claw Deformity of Feet 
 Aarskog syndrome +   
 acheiropody  
 acrocardiofacial syndrome 
 acrofacial dysostosis Rodriguez type 
 acrofacial dysostosis, Patagonia type 
 Acrootoocular Syndrome 
 acrorenal syndrome +  
 Anonychia-Ectrodactyly 
 Anonychia-Onychodystrophy with Hypoplasia or Absence of Distal Phalanges 
 Banki Syndrome 
 Bifid Femur with Monodactylous Ectrodactyly  
 brachydactyly type E1  
 brachydactyly type E2  
 Camptodactyly 1 
 Camptodactyly Joint Contractures and Facial Skeletal Dysplasia 
 Camptodactyly Syndrome Guadalajara Type +  
 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  
 Carnevale Hernandez Castillo Syndrome 
 Carpal Synostosis with Dysplastic Elbow Joints and Brachydactyly  
 Catel Manzke syndrome  
 Chitayat Meunier Hodgkinson Syndrome 
 Coffin-Siris syndrome +   
 cold-induced sweating syndrome +   
 Complex Camptosynpolydactyly  
 Cranioacrofacial Syndrome 
 Craniosynostosis, Adelaide Type 
 Daneman Davy Mancer Syndrome 
 Deafness, Congenital Onychodystrophy, Recessive Form 
 distal arthrogryposis type 1 +   
 distal arthrogryposis type 3  
 Distal Symphalangism +   
 DOORS syndrome  
 Dwarfism Stiff Joint Ocular Abnormalities 
 Dystelephalangy 
 ectodermal dysplasia, ectrodactyly, and macular dystrophy 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 
 Eiken syndrome  
 Extensor Tendons of Fingers, Anomalous Insertion of 
 Facial Dysmorphism, Cleft Palate, Hearing Loss, and Camptodactyly 
 Fairbank Disease 
 Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome 
 Frints De Smet Fabry Fryns Syndrome 
 Frontootopalatodigital Osteodysplasia 
 Fuhrmann syndrome  
 Gingival Fibromatosis with Hypertrichosis and Mental Retardation 
 Goodman Camptodactyly 
 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 
 Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate  
 hydrolethalus syndrome +   
 IVIC syndrome  
 Johnson Munson Syndrome 
 Keutel Syndrome  
 Khalifa Graham Syndrome 
 Laurin-Sandrow syndrome  
 Leri Pleonosteosis 
 Macrodactyly of the Hand 
 Mammary-Digital-Nail Syndrome 
 Metaphyseal Acroscyphodysplasia 
 Michels Caskey Syndrome 
 Microcephaly with Mental Retardation and Digital Anomalies  
 Mononen-Karnes-Senac syndrome 
 Morillo-Cucci Passarge Syndrome 
 Muller Barth Menger Syndrome 
 Neurofaciodigitorenal Syndrome 
 Odontotrichoungual-Digital-Palmar Syndrome 
 Oroacral Syndrome, Verloes-Koulischer Type 
 Oslam syndrome 
 otopalatodigital syndrome 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 
 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 
 Saal Bulas Syndrome 
 Sanderson Fraser 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 
 Stoll Alembik Dott Syndrome 
 Symphalangism with Multiple Anomalies of Hands and Feet 
 Symphalangism, C. S. Lewis Type 
 syndactyly type 8  
 Synpolydactyly 2  
 Tabatznik Syndrome 
 tarsal-carpal coalition syndrome +   
 Teebi hypertelorism syndrome +   
 Teebi Kaurah Syndrome 
 Tel Hashomer Camptodactyly Syndrome 
 terminal osseous dysplasia  
 Tollner Horst Manzke Syndrome 
 trichorhinophalangeal syndrome type III  
 Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet 
 Triphalangeal Thumb +   
 Tukel syndrome 
 Unilateral Adactylia 
 Unilateral Aplasia of Extensor Muscles of Fingers, with Generalized Polyneuropathy 
 Van Maldergem syndrome +   
 Ventricular Extrasystoles Perodactyly Robin Sequence 
 Vohwinkel syndrome  
 Walbaum Titran Durieux Crepin Syndrome 
 Weaver syndrome  
 Weyers Ulnar Ray/Oligodactyly Syndrome 
 Zimmerman Laband Syndrome +   

Synonyms
Exact Synonyms: Congenital Hand Deformity
Narrow Synonyms: HAND OLIGODACTYLY ;   OLIGODACTYLY (HANDS)
Primary IDs: MESH:D006228
Definition Sources: MESH:D006228

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