foot deformities, congenital

Preferred Label : foot deformities, congenital;

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

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

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

Details

Origin ID

D005532;

UMLS CUI

C0016508;

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)
- Congenital anomaly of toe (disorder) [SNOMED CT concept]
- Congenital valgus deformity of foot (disorder) [SNOMED CT concept]
- Foot deformity [MedDRA Preferred Term]
- Malformation foot NOS [MedDRA LLT]
- Other congenital deformities of feet [ICD-9 code]
Currated CISMeF NLP mapping
- Congenital abnormality of foot and toes (disorder) [SNOMED CT concept]
- Congenital deformities of feet [ICD-10 category]
- Congenital deformities of feet [ICD-11 Category]
- Congenital deformities of feet [ICD-10 category (who)]
- Congenital deformity of feet, unspecified [ICD-10 Sub-category (who)]
- Congenital deformity of feet, unspecified [ICD-10 Sub-category]
- Congenital deformity of foot (disorder) [SNOMED CT concept]
- Congenital foot malformation [MedDRA Preferred Term]
- Congenital foot malformation NOS [MedDRA LLT]
- MALFORMATION FOOT [WHO-ART Preferred Term]
- Malformation foot [MedDRA LLT]
- Other congenital deformities of feet [ICD-10 Sub-category (who)]
- congenital anomaly of foot, nos [SNOMED Notion]
- foot malformation [Disease (Nov.)]
Mapping VCM hiérarchique
- deformity [VCM modifier]
MeSH Descriptor(s) used for indexing
- foot [MeSH Descriptor]
- foot deformities [MeSH Descriptor]
Metaterm(s)
- podiatry [CISMeF Metaterm]
Record concept(s)
- foot deformities, congenital [MeSH concept]
Related MeSH Supplementary Concept(s)
- Brachyphalangy, polydactyly, and tibial aplasia-hypoplasia [MeSH Supplementary Concept]
- CAPOS syndrome [MeSH Supplementary Concept]
- Charcot-Marie-Tooth disease, foot deformity of [MeSH Supplementary Concept]
- Ectrodactyly and Ectodermal Dysplasia without Cleft Lip-Palate [MeSH Supplementary Concept]
- Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip-Palate Syndrome 3 [MeSH Supplementary Concept]
- Jackson-Weiss syndrome [MeSH Supplementary Concept]
- Laurin-Sandrow syndrome [MeSH Supplementary Concept]
- NOG-Related-Symphalangism spectrum disorder [MeSH Supplementary Concept]
- Odontotrichoungual-Digital-Palmar syndrome [MeSH Supplementary Concept]
- Split-Hand-Foot Malformation With Sensorineural Hearing Loss [MeSH Supplementary Concept]
- Zechi-Ceide syndrome [MeSH Supplementary Concept]
- acheiropodia [MeSH Supplementary Concept]
- acrootoocular syndrome [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]
- camptosynpolydactyly, complex [MeSH Supplementary Concept]
- cleft palate, deafness, and oligodontia [MeSH Supplementary Concept]
- craniosynostosis, adelaide type [MeSH Supplementary Concept]
- daneman davy mancer syndrome [MeSH Supplementary Concept]
- deafness, congenital onychodystrophy, recessive form [MeSH Supplementary Concept]
- digitotalar dysmorphism [MeSH Supplementary Concept]
- eiken skeletal dysplasia [MeSH Supplementary Concept]
- fairbank disease [MeSH Supplementary Concept]
- fibular aplasia, tibial campomelia, and oligosyndactyly syndrome [MeSH Supplementary Concept]
- frias syndrome [MeSH Supplementary Concept]
- fried goldberg mundel syndrome [MeSH Supplementary Concept]
- frints de smet fabry fryns syndrome [MeSH Supplementary Concept]
- fuhrmann syndrome [MeSH Supplementary Concept]
- game friedman paradice syndrome [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]
- johnson munson syndrome [MeSH Supplementary Concept]
- macrodactyly of the foot [MeSH Supplementary Concept]
- metatarsus varus, type I [MeSH Supplementary Concept]
- microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism [MeSH Supplementary Concept]
- mononen karnes senac syndrome [MeSH Supplementary Concept]
- monophalangy of great toe [MeSH Supplementary Concept]
- nicolaides baraitser syndrome [MeSH Supplementary Concept]
- oculodentodigital dysplasia [MeSH Supplementary Concept]
- oslam syndrome [MeSH Supplementary Concept]
- pfeiffer tietze welte syndrome [MeSH Supplementary Concept]
- polydactyly, postaxial, with dental and vertebral anomalies [MeSH Supplementary Concept]
- radial defect robin sequence [MeSH Supplementary Concept]
- radio-ulnar synostosis type 1 [MeSH Supplementary Concept]
- radio-ulnar synostosis type 2 [MeSH Supplementary Concept]
- ray peterson scott syndrome [MeSH Supplementary Concept]
- richieri costa Guion-Almeida syndrome [MeSH Supplementary Concept]
- sandhaus Ben-Ami syndrome [MeSH Supplementary Concept]
- second Metatarsal-Metacarpal syndrome [MeSH Supplementary Concept]
- split hand split foot nystagmus [MeSH Supplementary Concept]
- stoll alembik dott syndrome [MeSH Supplementary Concept]
- symphalangism with multiple anomalies of hands and feet [MeSH Supplementary Concept]
- symphalangism, distal [MeSH Supplementary Concept]
- synpolydactyly 2 [MeSH Supplementary Concept]
- synpolydactyly with foot anomalies [MeSH Supplementary Concept]
- talonavicular coalition [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]
- ulnar hypoplasia lobster claw deformity of feet [MeSH Supplementary Concept]
- van maldergem wetzburger verloes syndrome [MeSH Supplementary Concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital deformities of feet [ICD-10 category]
- Congenital deformities of feet [ICD-10 category (who)]
- Congenital deformities of feet [ICD-11 Category]
- Congenital deformity of feet, unspecified [ICD-10 Sub-category]
- Congenital deformity of feet, unspecified [ICD-10 Sub-category (who)]
- Congenital deformity of foot (disorder) [SNOMED CT concept]
- Congenital foot malformation [MedDRA Preferred Term]
- Congenital foot malformation NOS [MedDRA LLT]
- MALFORMATION FOOT [WHO-ART Preferred Term]
- Malformation foot [MedDRA LLT]
- Malformation foot NOS [MedDRA LLT]
- congenital anomaly of foot, nos [SNOMED Notion]
- foot malformation [Disease (Nov.)]
Validated automatic mappings to BTNT
- Congenital deformity of toe (disorder) [SNOMED CT concept]

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