chromosome 10q26 deletion syndrome

Preferred Label : chromosome 10q26 deletion syndrome;

MeSH synonym : terminal chromosome 10q26 deletion syndrome;

Origin ID

C567182;

UMLS CUI

C2674937;

Automatic exact mappings (from CISMeF team)
- distal 10q deletion syndrome [DO Concept]
Currated CISMeF NLP mapping
- Chromosome 10q26 deletion syndrome [OMIM Phenotype]
DO Cross reference
- distal 10q deletion syndrome [DO Concept]
MeSH term(s) associated for indexing
- Learning Disabilities [MeSH Descriptor]
- chromosome deletion [MeSH Descriptor]
- chromosomes, human, pair 10 [MeSH Descriptor]
- facies [MeSH Descriptor]
Record concept(s)
- chromosome 10q26 deletion syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Chromosome 10q26 deletion syndrome [OMIM Phenotype]
- Distal monosomy 10q [ORDO Disease]