polydactyly - CISMeF

Preferred Label : polydactyly;

MeSH definition : A congenital anomaly of the hand or foot, marked by the presence of supernumerary digits.;

MeSH synonym : hyperdactylies; polydactylias; hyperdactyly; polydactylies; polydactylia; polydactylism; polydactylisms;

MeSH annotation : do not confuse with SYNDACTYLY; coord IM with FINGERS /abnorm (IM) or TOES /abnorm (IM); SHORT RIB-POLYDACTYLY SYNDROME is also available;

Wikipedia link : https://en.wikipedia.org/wiki/Polydactyly;

Details

Origin ID

D017689;

UMLS CUI

C0152427;

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)
- With polydactyly [ACR pathology]
- With polydactyly [ACR pathology]
- With polydactyly [ACR pathology]
- With polydactyly [ACR pathology]
- With polydactyly [ACR pathology]
Currated CISMeF NLP mapping
- Hand polydactyly [HPO term]
- Non-syndromic polydactyly [ORDO Disease]
- POLYDACTYLY [WHO-ART Preferred Term]
- Polydactyly [ICD-10 category]
- Polydactyly [PASCAL descriptor]
- Polydactyly [MedDRA Preferred Term]
- Polydactyly [ICD-10 category (who)]
- Polydactyly [ICD-11 Category]
- Polydactyly [ICD-9 code]
- Polydactyly [NCIt concept]
- Polydactyly [OMIM Phenotype]
- Polydactyly [HPO term]
- Polydactyly (disorder) [SNOMED CT concept]
- Polydactyly, unspecified [ICD-10 Sub-category (who)]
- Polydactyly, unspecified [ICD-10 Sub-category]
- polydactyly [Disease (Nov.)]
- polydactyly [DO Concept]
- polydactyly, nos [SNOMED Notion]
DO Cross reference
- polydactyly [DO Concept]
False automatic mappings
- Foot polydactyly [HPO term]
HPO term
- Polydactyly [HPO term]
Manual NTBT mappings (CISMeF)
- Non-syndromic limb malformation [ORDO Disease]
- Non-syndromic polydactyly, syndactyly and/or hyperphalangy [ORDO Disease]
Ne pas confondre avec
- syndactyly [MeSH Descriptor]
ORDO relation(s)
- Non-syndromic polydactyly [ORDO Disease]
Record concept(s)
- polydactyly [MeSH concept]
Related MeSH Supplementary Concept(s)
- Brachyphalangy, polydactyly, and tibial aplasia-hypoplasia [MeSH Supplementary Concept]
- Kozlowski-Krajewska syndrome [MeSH Supplementary Concept]
- McKusick kaufman syndrome [MeSH Supplementary Concept]
- Meckel-Like cerebrorenodigital syndrome [MeSH Supplementary Concept]
- Megalancephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome [MeSH Supplementary Concept]
- Syndactyly-Polydactyly-Earlobe syndrome [MeSH Supplementary Concept]
- absence of tibia with polydactyly [MeSH Supplementary Concept]
- biemond syndrome II [MeSH Supplementary Concept]
- cortical blindness, retardation, and postaxial polydactyly [MeSH Supplementary Concept]
- crossed polydactyly, type I [MeSH Supplementary Concept]
- dandy walker malformation postaxial polydactyly [MeSH Supplementary Concept]
- desbuquois syndrome [MeSH Supplementary Concept]
- ectodermal dysplasia alopecia preaxial polydactyly [MeSH Supplementary Concept]
- ectodermal dysplasia syndrome with distinctive facial appearance and preaxial polydactyly of feet [MeSH Supplementary Concept]
- garret tripp syndrome [MeSH Supplementary Concept]
- hirschsprung disease polydactyly heart disease [MeSH Supplementary Concept]
- hirschsprung disease with heart defects, laryngeal anomalies, and preaxial polydactyly [MeSH Supplementary Concept]
- hirschsprung disease with polydactyly, renal agenesis, and deafness [MeSH Supplementary Concept]
- hirschsprung disease with ulnar polydactyly, polysyndactyly of big toes, and ventricular septal defect [MeSH Supplementary Concept]
- holoprosencephaly 9 [MeSH Supplementary Concept]
- hydrolethalus syndrome 1 [MeSH Supplementary Concept]
- laurence prosser rocker syndrome [MeSH Supplementary Concept]
- liver fibrocystic disease and polydactyly [MeSH Supplementary Concept]
- maroteaux fonfria syndrome [MeSH Supplementary Concept]
- meckel syndrome, type 4 [MeSH Supplementary Concept]
- mexican cardiomelic dysplasia [MeSH Supplementary Concept]
- oliver syndrome [MeSH Supplementary Concept]
- pfeiffer mayer syndrome [MeSH Supplementary Concept]
- polydactyly myopia syndrome [MeSH Supplementary Concept]
- polydactyly preaxial type 1 [MeSH Supplementary Concept]
- polydactyly, postaxial [MeSH Supplementary Concept]
- polydactyly, postaxial, type A2 [MeSH Supplementary Concept]
- polydactyly, postaxial, type A3 [MeSH Supplementary Concept]
- polydactyly, postaxial, type A4 [MeSH Supplementary Concept]
- polydactyly, postaxial, with dental and vertebral anomalies [MeSH Supplementary Concept]
- polydactyly, preaxial 4 [MeSH Supplementary Concept]
- polydactyly, preaxial III [MeSH Supplementary Concept]
- polysyndactyly, crossed [MeSH Supplementary Concept]
- preaxial deficiency, postaxial polydactyly and hypospadias [MeSH Supplementary Concept]
- preaxial hallucal polydactyly [MeSH Supplementary Concept]
- pseudotrisomy 13 syndrome [MeSH Supplementary Concept]
- santos mateus leal syndrome [MeSH Supplementary Concept]
- santos syndrome [MeSH Supplementary Concept]
- scalp defects postaxial polydactyly [MeSH Supplementary Concept]
- syndactyly, type IV [MeSH Supplementary Concept]
- synpolydactyly 2 [MeSH Supplementary Concept]
- synpolydactyly 3 [MeSH Supplementary Concept]
- synpolydactyly with foot anomalies [MeSH Supplementary Concept]
- thai symphalangism syndrome [MeSH Supplementary Concept]
- tibia absent polydactyly arachnoid cyst [MeSH Supplementary Concept]
- tibia, absence or hypoplasia of, with polydactyly, retrocerebellar arachnoid cyst, and other anomalies [MeSH Supplementary Concept]
- tibia, hypoplasia of, with polydactyly [MeSH Supplementary Concept]
- ulnar ray dysgenesis with postaxial polydactyly and renal cystic dysplasia [MeSH Supplementary Concept]
- urioste Martinez-Frias syndrome [MeSH Supplementary Concept]
See also
- syndactyly [MeSH Descriptor]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Multiple digits [MedDRA LLT]
- Non-syndromic polydactyly [ORDO Disease]
- POLYDACTYLY [WHO-ART Preferred Term]
- Polydactyly [ICD-9 code]
- Polydactyly [OMIM Phenotype]
- Polydactyly [ICD-10 category]
- Polydactyly [HPO term]
- Polydactyly [MedDRA Preferred Term]
- Polydactyly [ICD-10 category (who)]
- Polydactyly [NCIt concept]
- Polydactyly (disorder) [SNOMED CT concept]
- Polydactyly, unspecified [ICD-10 Sub-category]
- Polydactyly, unspecified [ICD-10 Sub-category (who)]
- Polydactyly, unspecified digits [MedDRA LLT]
- Polydactyly, unspecified digits [ICD-9 code]
- polydactyly [DO Concept]
- polydactyly [Disease (Nov.)]
- polydactyly, nos [SNOMED Notion]

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