Zinc finger, mym-type 2

Preferred Label : Zinc finger, mym-type 2;

Symbol : ZMYM2;

CISMeF acronym : ZMYM2;

Type : Gene;

Alternative titles and symbols : Zinc finger protein 198; Rearranged in atypical myeloproliferative disorder; Fused in myeloproliferative disorders; ZNF198; RAMP; FIM;

Included titles and symbols : Znf198/fgfr1 fusion gene;

Ensembl ID : ENSG00000121741;

Prefixed ID : *602221;

Details

Origin ID

602221;

UMLS CUI

C1823958;

Automatic exact mappings (from CISMeF team)
- Assistive products for vertical accessibility, other and unspecified [ICHI extension code]
- DTL wt Allele [NCIt concept]
- O-beta-ribosyl(1''--2')adenosine-5''-phosphate [MeSH Supplementary Concept]
- Ramp (physical object) [SNOMED CT concept]
- Ramping (qualifier value) [SNOMED CT concept]
- ZMYM2 Gene [NCIt concept]
- ZMYM2 wt Allele [NCIt concept]
- ZMYM2/FGFR1 Fusion Gene [NCIt concept]
- Zinc Finger MYM-Type Protein 2 [NCIt concept]
- architectural accessibility [MeSH Descriptor]
- congenital myasthenic syndrome 6 [DO Concept]
- ramps [MeSH concept]
- ramps [EMDN type]
- zinc finger MYM-type containing 2 [HGNC gene]
HGNC gene
- zinc finger MYM-type containing 2 [HGNC gene]
NCIt concept(s)
- ZMYM2 Gene [NCIt concept]
- ZMYM2 wt Allele [NCIt concept]
- Zinc Finger MYM-Type Protein 2 [NCIt concept]
ORDO concept(s)
- zinc finger MYM-type containing 2 [ORDO Gene]
Phenotypes related
- Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- ZMYM2 Gene [NCIt concept]
- zinc finger MYM-type containing 2 [HGNC gene]

Keyword's position in hierarchy(ies) :

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