Synpolydactyly 3

Preferred Label : Synpolydactyly 3;

Symbol : SPD3;

CISMeF acronym : SPD3;

Type : Phenotype or locus, molecular basis unknown;

Description : For a general phenotypic description and a discussion of genetic heterogeneity of synpolydactyly, see SPD1 (186000).;

Prefixed ID : %610234;

Details

Origin ID

610234;

UMLS CUI

C1853255;

Currated CISMeF NLP mapping
- Synpolydactyly type 3 [ORDO Disease]
- synpolydactyly 3 [MeSH concept]
- synpolydactyly 3 [MeSH Supplementary Concept]
DO Cross reference
- synpolydactyly [DO Concept]
ORDO concept(s)
- Syndactyly type 2 [ORDO Disease]
- Synpolydactyly type 3 [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Synpolydactyly type 3 [ORDO Disease]
- synpolydactyly 3 [MeSH Supplementary Concept]
- synpolydactyly 3 [MeSH concept]

Keyword's position in hierarchy(ies) :

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