syndactyly - CISMeF

Preferred Label : syndactyly;

MeSH definition : A congenital anomaly of the hand or foot, marked by the webbing between adjacent fingers or toes. Syndactylies are classified as complete or incomplete by the degree of joining. Syndactylies can also be simple or complex. Simple syndactyly indicates joining of only skin or soft tissue; complex syndactyly marks joining of bony elements.;

MeSH synonym : syndactylias; syndactylies; syndactylia;

MeSH hyponym : polysyndactyly;

MeSH annotation : do not confuse with POLYDACTYLY; coord IM with FINGERS /abnorm (IM) or TOES /abnorm (IM); ACROCEPHALOSYNDACTYLIA is also available;

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

Details

Origin ID

D013576;

UMLS CUI

C0039075;

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)
- 2-3 toe syndactyly [HPO term]
- Polysyndactyly [NCIt concept]
- Polysyndactyly [ICD-10 Sub-category (who)]
- Polysyndactyly [ORDO Disease]
- Polysyndactyly [MedDRA LLT]
- Polysyndactyly (disorder) [SNOMED CT concept]
- Polysyndactyly syndrome (disorder) [SNOMED CT concept]
- Polysyndactyly, unspecified [ICD-10 Sub-category]
- Syndactylization (procedure) [Inactive SNOMED CT concept]
- With polysyndactyly [ACR pathology]
- With polysyndactyly [ACR pathology]
- With polysyndactyly [ACR pathology]
- With polysyndactyly [ACR pathology]
- With polysyndactyly [ACR pathology]
- With syndactyly [ACR pathology]
- With syndactyly [ACR pathology]
- With syndactyly [ACR pathology]
- With syndactyly [ACR pathology]
- With syndactyly [ACR pathology]
- polysyndactyly [SNOMED Notion]
- syndactylization [SNOMED Notion]
Currated CISMeF NLP mapping
- Non-syndromic syndactyly [ORDO Disease]
- SYNDACTYLY [WHO-ART Preferred Term]
- Syndactyly [ICD-10 category]
- Syndactyly [PASCAL descriptor]
- Syndactyly [ICD-11 Category]
- Syndactyly [ICD-9 code]
- Syndactyly [ICD-10 category (who)]
- Syndactyly [HPO term]
- Syndactyly [MedDRA Preferred Term]
- Syndactyly [NCIt concept]
- Syndactyly (disorder) [SNOMED CT concept]
- Syndactyly, unspecified [ICD-10 Sub-category (who)]
- Syndactyly, unspecified [ICD-10 Sub-category]
- syndactyly [Disease (Nov.)]
- syndactyly [DO Concept]
- syndactyly [SNOMED Notion]
DO Cross reference
- syndactyly [DO Concept]
False automatic mappings
- Toe syndactyly [HPO term]
HPO term
- Syndactyly [HPO term]
Manual BTNT mappings - CISMeF
- Brachydactyly-syndactyly, Zhao type [ORDO Disease]
- Mesoaxial synostotic syndactyly with phalangeal reduction [ORDO Disease]
- Syndactyly type 1 [ORDO Disease]
- Syndactyly type 2 [ORDO Disease]
- Syndactyly type 3 [ORDO Disease]
- Syndactyly type 4 [ORDO Disease]
- Syndactyly type 5 [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Non-syndromic limb malformation [ORDO Disease]
- Non-syndromic polydactyly, syndactyly and/or hyperphalangy [ORDO Disease]
Ne pas confondre avec
- polydactyly [MeSH Descriptor]
ORDO relation(s)
- Non-syndromic syndactyly [ORDO Disease]
Record concept(s)
- polysyndactyly [MeSH concept]
- syndactyly [MeSH concept]
Related MeSH Supplementary Concept(s)
- Brachydactyly-Syndactyly syndrome [MeSH Supplementary Concept]
- Kozlowski-Krajewska syndrome [MeSH Supplementary Concept]
- Naguib-Richieri-Costa syndrome [MeSH Supplementary Concept]
- Rosselli-Gulienetti syndrome [MeSH Supplementary Concept]
- Syndactyly-Polydactyly-Earlobe syndrome [MeSH Supplementary Concept]
- Zlotogora-Ogur syndrome [MeSH Supplementary Concept]
- aphalangia syndactyly microcephaly [MeSH Supplementary Concept]
- arterial occlusive disease, progressive, with hypertension, heart defects, bone fragility, and brachysyndactyly [MeSH Supplementary Concept]
- aurocephalosyndactyly [MeSH Supplementary Concept]
- blepharophimosis with ptosis, syndactyly, and short stature [MeSH Supplementary Concept]
- bonneau syndrome [MeSH Supplementary Concept]
- ectodermal dysplasia mental retardation syndactyly [MeSH Supplementary Concept]
- eyebrows duplication of, with stretchable skin and syndactyly [MeSH Supplementary Concept]
- fibular aplasia, tibial campomelia, and oligosyndactyly syndrome [MeSH Supplementary Concept]
- filippi syndrome [MeSH Supplementary Concept]
- frints de smet fabry fryns syndrome [MeSH Supplementary Concept]
- gollop coates syndrome [MeSH Supplementary Concept]
- green sandford davison syndrome [MeSH Supplementary Concept]
- kleiner holmes syndrome [MeSH Supplementary Concept]
- lacrimoauriculodentodigital syndrome [MeSH Supplementary Concept]
- landy donnai syndrome [MeSH Supplementary Concept]
- martinez monasterio pinheiro syndrome [MeSH Supplementary Concept]
- oculodentodigital dysplasia [MeSH Supplementary Concept]
- oculodentodigital dysplasia, autosomal recessive [MeSH Supplementary Concept]
- oculodentoosseous dysplasia recessive [MeSH Supplementary Concept]
- orofacial cleft 7 [MeSH Supplementary Concept]
- orstavik lindemann solberg syndrome [MeSH Supplementary Concept]
- pavone fiumara rizzo syndrome [MeSH Supplementary Concept]
- pfeiffer rockelein syndrome [MeSH Supplementary Concept]
- piepkorn karp hickok syndrome [MeSH Supplementary Concept]
- polydactyly, postaxial, type A4 [MeSH Supplementary Concept]
- polysyndactyly, crossed [MeSH Supplementary Concept]
- popliteal pterygium syndrome [MeSH Supplementary Concept]
- popliteal pterygium syndrome, lethal type [MeSH Supplementary Concept]
- radio-ulnar synostosis type 1 [MeSH Supplementary Concept]
- radio-ulnar synostosis type 2 [MeSH Supplementary Concept]
- sclerosteosis [MeSH Supplementary Concept]
- scott bryant graham syndrome [MeSH Supplementary Concept]
- short stature, facial dysmorphism, severe brachydactyly, and syndactyly [MeSH Supplementary Concept]
- syndactyly cenani lenz type [MeSH Supplementary Concept]
- syndactyly, mesoaxial synostotic, with phalangeal reduction [MeSH Supplementary Concept]
- syndactyly, type 2 [MeSH Supplementary Concept]
- syndactyly, type 3 [MeSH Supplementary Concept]
- syndactyly, type I [MeSH Supplementary Concept]
- syndactyly, type IV [MeSH Supplementary Concept]
- syndactyly, type v [MeSH Supplementary Concept]
- timothy syndrome [MeSH Supplementary Concept]
- toe syndactyly, telecanthus, and anogenital and renal malformations [MeSH Supplementary Concept]
- trueb burg bottani syndrome [MeSH Supplementary Concept]
- winter shortland temple syndrome [MeSH Supplementary Concept]
- zerres rietschel majewski syndrome [MeSH Supplementary Concept]
- zygodactyly 1 [MeSH Supplementary Concept]
See also
- polydactyly [MeSH Descriptor]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Non-syndromic syndactyly [ORDO Disease]
- SYNDACTYLY [WHO-ART Preferred Term]
- Symphalangism [PASCAL descriptor]
- Symphalangism (disorder) [SNOMED CT concept]
- Syndactyly [ICD-9 code]
- Syndactyly [ICD-10 category]
- Syndactyly [MedDRA Preferred Term]
- Syndactyly [HPO term]
- Syndactyly [ICD-10 category (who)]
- Syndactyly [PASCAL descriptor]
- Syndactyly [ICD-11 Category]
- Syndactyly [NCIt concept]
- Syndactyly (disorder) [SNOMED CT concept]
- Syndactyly, unspecified [ICD-10 Sub-category]
- Syndactyly, unspecified [ICD-10 Sub-category (who)]
- symphalangy [SNOMED Notion]
- syndactyly [DO Concept]
- syndactyly [Disease (Nov.)]
- syndactyly [SNOMED Notion]
Validated automatic mappings to BTNT
- Polysyndactyly [ICD-11 Subcategory]

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