Ontology Browser

Term:
Upper Extremity Deformities, Congenital (DOID:9004402)
Annotations: Rat: (77) Mouse: (77) Human: (81) Chinchilla: (77) Bonobo: (75) Dog: (77) Squirrel: (76)
Parent Terms Term With Siblings Child Terms
Aase Smith Syndrome 
Abruzzo Erickson Syndrome  
Acromegaloid Facial Appearance Syndrome 
Acromesomelic Dysplasia, Demirhan Type  
Acromicric Dysplasia +   
Acropectoral Syndrome 
Acropectorovertebral Dysplasia 
Adams-Oliver syndrome +   
ADULT syndrome  
Agenesis of Corpus Callosum with Facial Anomalies and Robin Sequence 
Arachnodactyly +   
Atelosteogenesis Type 3  
autosomal recessive Robinow syndrome  
B-Cell Immunodeficiency, Distal Limb Anomalies, and Urogenital Malformations 
Bagatelle Cassidy syndrome 
brachydactyly +   
Brachymorphism-Onychodysplasia-Dysphalangism Syndrome 
Brachyolmia Type 1, Hobaek Type 
Calabro Syndrome 
Camptobrachydactyly 
Cartwright Nelson Fryns Syndrome 
Cerebrorenodigital Syndrome with Limb Malformations and Triradiate Acetabula 
CHILD Syndrome  
CHITAYAT SYNDROME  
cocoon syndrome  
CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY  
Craniomicromelic Syndrome 
Diaphragmatic Defects, Limb Deficiencies, and Ossification Defects Of Skull 
Ectrodactyly-Polydactyly 
Ectromelia +   
Faciocardiomelic Dysplasia, Lethal 
Feingold syndrome +   
Fetal Akinesia Syndrome, X-Linked 
Freire-Maia Odontotrichomelic Syndrome 
Fryns Syndrome 
Genee-Wiedemann Syndrome  
Grubben de Cock Borghgraef Syndrome 
Hand and Foot Deformity with Flat Facies 
Hanhart Syndrome 
Heart Defects Limb Shortening 
hypochondroplasia  
Hypoglossia-Hypodactylia 
Ichthyosis Tapered Fingers Midline Groove Up 
INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES  
Kaplan Plauchu Fitch Syndrome 
Kaufman Oculocerebrofacial Syndrome  
Kuster Syndrome 
Laryngeal Atresia, Encephalocele, and Limb Deformities 
Le Marec Bracq Picaud Syndrome 
Limb Defects, Distal Transverse, with Mental Retardation and Spasticity 
Limb-Mammary Syndrome  
Lower Extremity Deformities, Congenital +   
Lynch Lee Murday syndrome 
Malformation of Arms 
Megalodactyly  
Mental Retardation Spasticity Ectrodactyly 
Mesomelia-Synostoses Syndrome 
Metaphyseal Anadysplasia +   
Microphthalmia with Cyst, Bilateral Facial Clefts, and Limb Anomalies 
Microphthalmia, Syndromic 6  
Multiple Epiphyseal Dysplasia with Robin Phenotype 
Multiple Pterygium Syndrome, X-Linked 
Nephrosis Deafness Urinary Tract Digital Malformation 
Neu-Laxova syndrome 1  
Nievergelt Syndrome 
Palant Cleft Palate Syndrome 
Penttinen-Aula Syndrome  
Peters plus syndrome  
Pointer Syndrome 
polydactyly +   
Postaxial Oligodactyly, Tetramelic 
Powell Chandra Saal Syndrome 
Proteus syndrome +   
Radial Ray Deficiency, X-Linked 
Radiohumeral Fusions with Other Skeletal and Craniofacial Anomalies  
rapadilino syndrome  
Reardon Hall Slaney syndrome 
Renal Dysplasia - Limb Defects Syndrome 
Robinow syndrome +   
Ruzicka Goerz Anton syndrome 
Short Stature-Obesity Syndrome 
Splenogonadal Fusion Limb Defects Micrognatia 
split hand-foot malformation +   
SPLIT-FOOT MALFORMATION WITH MESOAXIAL POLYDACTYLY  
Split-Hand with Obstructive Uropathy, Spina Bifida, and Diaphragmatic Defects 
Split-Hand-Foot Malformation With Long Bone Deficiency 1 
Split-Hand/Foot Malformation with Long Bone Deficiency 2 
Split-Hand/Foot Malformation with Long Bone Deficiency 3 
Steinfeld Syndrome 
Stern Lubinsky Durrie Syndrome 
Stratton-Parker Syndrome 
syndactyly +   
Tetramelic Monodactyly 
thanatophoric dysplasia +   
Thoracic Dysplasia-Hydrocephalus Syndrome 
Thoraco Limb Dysplasia Rivera Type 
Thoracomelic Dysplasia 
Ulnar Hypoplasia with Mental Retardation 
Upper Extremity Deformities, Congenital +   
Congenital structural abnormalities of the UPPER EXTREMITY.
VACTERL association  
Viljoen Kallis Voges Syndrome 
Weill-Marchesani Syndrome 3  
Weyers Acrofacial Dysostosis  
Wright Dyck Syndrome 
Yunis-Varon syndrome  

Synonyms
Exact Synonyms: Upper Limb Deformities, Congenital
Primary IDs: MESH:D038062 ;   RDO:0000382
Definition Sources: MESH:D038062

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