hand deformities, congenital

Preferred Label : hand deformities, congenital;

MeSH definition : Alterations or deviations from normal shape or size which result in a disfigurement of the hand occurring at or before birth.;

MeSH synonym : congenital hand deformities; congenital hand deformity; deformities, congenital hand; deformity, congenital hand; hand deformity, congenital;

MeSH annotation : do not use /congen & do not coord with INFANT, NEWBORN, DISEASES;

Details

Origin ID

D006228;

UMLS CUI

C0018566;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Malformation hand NOS [MedDRA LLT]
Currated CISMeF NLP mapping
- Congenital Hand and Foot Deformity [NCIt concept]
- Congenital anomaly of hand (disorder) [SNOMED CT concept]
- Congenital deformities of fingers [ICD-11 Category]
- Congenital deformity of finger(s) and hand [ICD-10 Sub-category]
- Congenital deformity of hand [ICD-10 Sub-category (who)]
- Congenital deformity of hand (disorder) [SNOMED CT concept]
- Congenital hand malformation [MedDRA Preferred Term]
- Congenital hand malformation NOS [MedDRA LLT]
- MALFORMATION HAND [WHO-ART High Level Term]
- Malformation hand [MedDRA LLT]
- Malformation of hand [MedDRA LLT]
- congenital anomaly of the hand, nos [SNOMED Notion]
Mapping VCM hiérarchique
- deformity [VCM modifier]
MeSH Descriptor(s) used for indexing
- hand [MeSH Descriptor]
- hand deformities [MeSH Descriptor]
Record concept(s)
- hand deformities, congenital [MeSH concept]
Related MeSH Supplementary Concept(s)
- Aarskog syndrome [MeSH Supplementary Concept]
- Anonychia-Ectrodactyly [MeSH Supplementary Concept]
- CATSHL syndrome [MeSH Supplementary Concept]
- Coffin-Siris syndrome [MeSH Supplementary Concept]
- Ectrodactyly and Ectodermal Dysplasia without Cleft Lip-Palate [MeSH Supplementary Concept]
- Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip-Palate Syndrome 1 [MeSH Supplementary Concept]
- Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip-Palate Syndrome 3 [MeSH Supplementary Concept]
- Ectrodactyly-Cleft palate syndrome [MeSH Supplementary Concept]
- Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate [MeSH Supplementary Concept]
- Laurin-Sandrow syndrome [MeSH Supplementary Concept]
- Morillo-Cucci passarge syndrome [MeSH Supplementary Concept]
- NOG-Related-Symphalangism spectrum disorder [MeSH Supplementary Concept]
- Odontotrichoungual-Digital-Palmar syndrome [MeSH Supplementary Concept]
- Oto-Palato-digital syndrome type 1 [MeSH Supplementary Concept]
- Schinzel-Giedion syndrome [MeSH Supplementary Concept]
- Split-Hand-Foot Malformation With Sensorineural Hearing Loss [MeSH Supplementary Concept]
- Weaver-Like syndrome [MeSH Supplementary Concept]
- Weyers ulnar ray-oligodactyly syndrome [MeSH Supplementary Concept]
- acheiropodia [MeSH Supplementary Concept]
- acrofacial dysostosis rodriguez type [MeSH Supplementary Concept]
- acrofacial dysostosis, palagonia type [MeSH Supplementary Concept]
- acrootoocular syndrome [MeSH Supplementary Concept]
- acrorenal syndrome [MeSH Supplementary Concept]
- adactylia, unilateral [MeSH Supplementary Concept]
- anonychia-onychodystrophy with hypoplasia or absence of distal phalanges [MeSH Supplementary Concept]
- aphalangia, partial, with syndactyly and duplication of metatarsal IV [MeSH Supplementary Concept]
- aplasia of extensor muscles of fingers, unilateral, with generalized polyneuropathy [MeSH Supplementary Concept]
- banki syndrome [MeSH Supplementary Concept]
- camptodactyly 1 [MeSH Supplementary Concept]
- camptodactyly joint contractures and facial skeletal dysplasia [MeSH Supplementary Concept]
- camptodactyly syndrome guadalajara type 1 [MeSH Supplementary Concept]
- camptodactyly syndrome guadalajara type 2 [MeSH Supplementary Concept]
- camptodactyly taurinuria [MeSH Supplementary Concept]
- camptodactyly vertebral fusion [MeSH Supplementary Concept]
- camptodactyly, fibrous tissue hyperplasia, and skeletal dysplasia [MeSH Supplementary Concept]
- camptodactyly-ichthyosis syndrome [MeSH Supplementary Concept]
- camptosynpolydactyly, complex [MeSH Supplementary Concept]
- carnevale hernandez castillo syndrome [MeSH Supplementary Concept]
- catel manzke syndrome [MeSH Supplementary Concept]
- cleft palate, cardiac defect, genital anomalies, and ectrodactyly [MeSH Supplementary Concept]
- cranioacrofacial syndrome [MeSH Supplementary Concept]
- craniosynostosis, adelaide type [MeSH Supplementary Concept]
- crisponi syndrome [MeSH Supplementary Concept]
- daneman davy mancer syndrome [MeSH Supplementary Concept]
- deafness, congenital onychodystrophy, recessive form [MeSH Supplementary Concept]
- digitorenocerebral syndrome [MeSH Supplementary Concept]
- digitotalar dysmorphism [MeSH Supplementary Concept]
- dwarfism stiff joint ocular abnormalities [MeSH Supplementary Concept]
- dystelephalangy [MeSH Supplementary Concept]
- ectodermal dysplasia, ectrodactyly, and macular dystrophy [MeSH Supplementary Concept]
- eiken skeletal dysplasia [MeSH Supplementary Concept]
- facial dysmorphism, cleft palate, hearing loss, and camptodactyly [MeSH Supplementary Concept]
- fairbank disease [MeSH Supplementary Concept]
- femur bifid with monodactylous ectrodactyly [MeSH Supplementary Concept]
- fibromatosis, gingival, with hypertrichosis and mental retardation [MeSH Supplementary Concept]
- fibular aplasia, tibial campomelia, and oligosyndactyly syndrome [MeSH Supplementary Concept]
- frints de smet fabry fryns syndrome [MeSH Supplementary Concept]
- frontootopalatodigital osteodysplasia [MeSH Supplementary Concept]
- fuhrmann syndrome [MeSH Supplementary Concept]
- goodman camptodactyly [MeSH Supplementary Concept]
- gordon syndrome [MeSH Supplementary Concept]
- growth mental deficiency syndrome of myhre [MeSH Supplementary Concept]
- growth retardation, small and puffy hands and feet, and eczema [MeSH Supplementary Concept]
- hairy palms and soles [MeSH Supplementary Concept]
- hand foot uterus syndrome [MeSH Supplementary Concept]
- heart-hand syndrome, slovenian type [MeSH Supplementary Concept]
- hecht scott syndrome [MeSH Supplementary Concept]
- hydrolethalus syndrome [MeSH Supplementary Concept]
- jacobs syndrome [MeSH Supplementary Concept]
- johnson munson syndrome [MeSH Supplementary Concept]
- keutel syndrome [MeSH Supplementary Concept]
- leri pleonosteosis [MeSH Supplementary Concept]
- macrodactyly of the hand [MeSH Supplementary Concept]
- metacarpal 4 5 fusion [MeSH Supplementary Concept]
- metaphyseal acroscyphodysplasia [MeSH Supplementary Concept]
- michels caskey syndrome [MeSH Supplementary Concept]
- microcephaly with mental retardation and digital anomalies [MeSH Supplementary Concept]
- mononen karnes senac syndrome [MeSH Supplementary Concept]
- muller barth menger syndrome [MeSH Supplementary Concept]
- neurofaciodigitorenal syndrome [MeSH Supplementary Concept]
- oculootoradial syndrome [MeSH Supplementary Concept]
- oroacral syndrome, Verloes-Koulischer type [MeSH Supplementary Concept]
- oslam syndrome [MeSH Supplementary Concept]
- oto-palato-digital syndrome, type 2 [MeSH Supplementary Concept]
- otopalatodigital spectrum disorder [MeSH Supplementary Concept]
- patent ductus arteriosus and bicuspid aortic valve with hand anomalies [MeSH Supplementary Concept]
- pfeiffer tietze welte syndrome [MeSH Supplementary Concept]
- polydactyly, postaxial, with dental and vertebral anomalies [MeSH Supplementary Concept]
- progeroid facial appearance with hand anomalies [MeSH Supplementary Concept]
- pseudotrisomy 13 syndrome [MeSH Supplementary Concept]
- pterygium colli mental retardation digital anomalies [MeSH Supplementary Concept]
- radio-ulnar synostosis type 1 [MeSH Supplementary Concept]
- radio-ulnar synostosis type 2 [MeSH Supplementary Concept]
- rhizomelic dysplasia patterson lowry type [MeSH Supplementary Concept]
- richieri costa Guion-Almeida syndrome [MeSH Supplementary Concept]
- richieri costa pereira syndrome [MeSH Supplementary Concept]
- rozin hertz goodman syndrome [MeSH Supplementary Concept]
- saal bulas syndrome [MeSH Supplementary Concept]
- sanderson fraser syndrome [MeSH Supplementary Concept]
- say field coldwell syndrome [MeSH Supplementary Concept]
- second Metatarsal-Metacarpal syndrome [MeSH Supplementary Concept]
- split hand split foot nystagmus [MeSH Supplementary Concept]
- spondylocamptodactyly [MeSH Supplementary Concept]
- stoll alembik dott syndrome [MeSH Supplementary Concept]
- symphalangism with multiple anomalies of hands and feet [MeSH Supplementary Concept]
- symphalangism, C. S. lewis type [MeSH Supplementary Concept]
- symphalangism, distal [MeSH Supplementary Concept]
- synostosis, carpal, with dysplastic elbow joints and brachydactyly [MeSH Supplementary Concept]
- synpolydactyly 2 [MeSH Supplementary Concept]
- tabatznik syndrome [MeSH Supplementary Concept]
- teebi kaurah syndrome [MeSH Supplementary Concept]
- tel hashomer camptodactyly syndrome [MeSH Supplementary Concept]
- tollner horst manzke syndrome [MeSH Supplementary Concept]
- trichorhinophalangeal syndrome, type III [MeSH Supplementary Concept]
- trigonobrachycephaly, bulbous bifid nose, micrognathia, and abnormalities of the hands and feet [MeSH Supplementary Concept]
- triphalangeal thumb [MeSH Supplementary Concept]
- triphalangeal thumb non opposable [MeSH Supplementary Concept]
- triphalangeal thumb with double phalanges [MeSH Supplementary Concept]
- tukel syndrome [MeSH Supplementary Concept]
- van maldergem wetzburger verloes syndrome [MeSH Supplementary Concept]
- ventricular extrasystoles perodactyly robin sequence [MeSH Supplementary Concept]
- vohwinkel syndrome [MeSH Supplementary Concept]
- walbaum titran durieux crepin syndrome [MeSH Supplementary Concept]
- weaver syndrome [MeSH Supplementary Concept]
- zimmerman laband syndrome [MeSH Supplementary Concept]
See also (suggested by CISMeF)
- hand deformities [MeSH Descriptor]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital anomaly of hand (disorder) [SNOMED CT concept]
- Congenital deformities of fingers [ICD-11 Category]
- Congenital deformity of hand [ICD-10 Sub-category (who)]
- Congenital deformity of hand (disorder) [SNOMED CT concept]
- Congenital hand malformation [MedDRA Preferred Term]
- Congenital hand malformation NOS [MedDRA LLT]
- congenital anomaly of the hand, nos [SNOMED Notion]
Validated automatic mappings to NTBT
- hand malformation [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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