Chromosome 2q31.2 deletion syndrome

Preferred Label : Chromosome 2q31.2 deletion syndrome;

Type : Phenotype, molecular basis known;

Prefixed ID : #612345;

Origin ID

612345;

UMLS CUI

C2676724;

Currated CISMeF NLP mapping
- chromosome 2q31.2 deletion syndrome [DO Concept]
- chromosome 2q31.2 deletion syndrome [MeSH concept]
- chromosome 2q31.2 deletion syndrome [MeSH Supplementary Concept]
DO Cross reference
- chromosome 2q31.2 deletion syndrome [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- chromosome 2q31.2 deletion syndrome [MeSH Supplementary Concept]
- chromosome 2q31.2 deletion syndrome [MeSH concept]
- chromosome 2q31.2 deletion syndrome [DO Concept]