chromosome 2q37 deletion syndrome

Preferred Label : chromosome 2q37 deletion syndrome;

MeSH synonym : monosomy 2q37; deletion 2q37; Brachydactyly-Mental retardation syndrome; 2q37 deletion syndrome; albright hereditary osteodystrophy-like syndrome; chromosome 2, monosomy 2q37;

Is substance : O;

Détails

Origin ID

C538317;

UMLS CUI

C2931817;

CISMeF manual mappings
- 2q37 microdeletion syndrome [ORDO Disease]
- Chromosome 2q37 deletion syndrome (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- 2q37 deletion [ICD-11 More detail]
- Chromosome 2q37 Deletion Syndrome [NCIt concept]
- Chromosome 2q37 deletion syndrome [OMIM Phenotype]
- chromosome 2q37 deletion syndrome [DO Concept]
DO Cross reference
- chromosome 2q37 deletion syndrome [DO Concept]
MeSH term(s) associated for indexing
- chromosome deletion [MeSH Descriptor]
- chromosomes, human, pair 2 [MeSH Descriptor]
ORDO relation(s)
- 2q37 microdeletion syndrome [ORDO Disease]
Record concept(s)
- chromosome 2q37 deletion syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- 2q37 deletion [ICD-11 More detail]
- 2q37 microdeletion syndrome [ORDO Disease]
- Chromosome 2q37 Deletion Syndrome [NCIt concept]
- Chromosome 2q37 deletion syndrome [OMIM Phenotype]
- Chromosome 2q37 deletion syndrome (disorder) [SNOMED CT concept]
- chromosome 2q37 deletion syndrome [DO Concept]

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