chromosome 19q13.11 deletion syndrome

Preferred Label : chromosome 19q13.11 deletion syndrome;

Origin ID

C567810;

UMLS CUI

C2751651;

CISMeF manual mappings
- 19q13.11 microdeletion syndrome (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- 19q13.11 deletion [ICD-11 More detail]
- 19q13.11 microdeletion syndrome [ORDO Disease]
- Chromosome 19q13.11 deletion syndrome, distal [OMIM Phenotype]
- chromosome 19q13.11 deletion syndrome [DO Concept]
DO Cross reference
- chromosome 19q13.11 deletion syndrome [DO Concept]
MeSH term(s) associated for indexing
- abnormalities, multiple [MeSH Descriptor]
- chromosome deletion [MeSH Descriptor]
- chromosome disorders [MeSH Descriptor]
Record concept(s)
- chromosome 19q13.11 deletion syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- 19q13.11 microdeletion syndrome [ORDO Disease]
- chromosome 19q13.11 deletion syndrome [DO Concept]