Syndactyly, type III

Preferred Label : Syndactyly, type III;

Symbol : SDTY3;

CISMeF acronym : SDTY3;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Ring and little finger syndactyly; Syndactyly of fingers iv and V;

Inheritance : Autosomal dominant;

Prefixed ID : #186100;

Détails

Origin ID

186100;

UMLS CUI

C1861366;

Automatic exact mappings (from CISMeF team)
- Syndactyly type 3 [ICD-11 More detail]
- Syndactyly type 3 (disorder) [SNOMED CT concept]
- Syndactyly, type v [MeSH concept]
- gap junction protein alpha 1 [ORDO Gene]
- syndactyly type 3 [DO Concept]
- syndactyly, type v [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- Syndactyly type 3 [ORDO Disease]
- Syndactyly, type 3 [MeSH concept]
- syndactyly, type 3 [MeSH Supplementary Concept]
DO Cross reference
- syndactyly type 3 [DO Concept]
Genes related to phenotype
- Gap junction protein, alpha-1 [OMIM gene]
HPO term(s)
- 4-5 finger syndactyly [HPO term]
- Absent middle phalanx of 5th finger [HPO term]
- Autosomal dominant inheritance [HPO term]
- Short 5th finger [HPO term]
- Short 5th finger with absent/rudimentary middle phalanx [HPO term]
- Syndactyly [HPO term]
Not associated HPO term(s)
- Toe syndactyly [HPO term]
ORDO concept(s)
- Syndactyly type 3 [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Syndactyly type 3 [ORDO Disease]
- Syndactyly type 3 (disorder) [SNOMED CT concept]
- Syndactyly, type 3 [MeSH concept]
- syndactyly type 3 [DO Concept]
- syndactyly, type 3 [MeSH Supplementary Concept]

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