Stuttering, familial persistent, 2

Preferred Label : Stuttering, familial persistent, 2;

Symbol : STUT2;

CISMeF acronym : STUT2;

Type : Phenotype or locus, molecular basis unknown;

Description : For a phenotypic description and a discussion of genetic heterogeneity of familial persistent stuttering, see 184450.;

Prefixed ID : %609261;

Details

Origin ID

609261;

UMLS CUI

C1836484;

Currated CISMeF NLP mapping
- stuttering, familial persistent 2 [MeSH concept]
- stuttering, familial persistent 2 [MeSH Supplementary Concept]
DO Cross reference
- stuttering [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- stuttering, familial persistent 2 [MeSH Supplementary Concept]
- stuttering, familial persistent 2 [MeSH concept]

Keyword's position in hierarchy(ies) :

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