Microphthalmia-associated transcription factor

Preferred Label : Microphthalmia-associated transcription factor;

Symbol : MITF;

CISMeF acronym : MITF;

Type : Gene;

Alternative titles and symbols : Microphthalmia, mouse, homolog of; MI;

Ensembl ID : ENSG00000187098;

Prefixed ID : *156845;

Détails

Origin ID

156845;

UMLS CUI

C1417172;

Automatic exact mappings (from CISMeF team)
- Family History of Myocardial Infarction [NCIt concept]
- MITF Gene [NCIt concept]
- MITF wt Allele [NCIt concept]
- Mebi [NCIt concept]
- Michigan [NCIt concept]
- Microphthalmia-Associated Transcription Factor [NCIt concept]
- Microphthalmia-Associated transcription factor [MeSH concept]
- Microscopic Findings Domain [NCIt concept]
- Mitral valve insufficiency [ICD-11 Category]
- Motivational Interviewing [NCIt concept]
- Myo-Inositol Measurement [NCIt concept]
- Myocardial Infarction [NCIt concept]
- Myocardial Infarction ECG Assessment [NCIt concept]
- Myocardial infarction [HPO term]
- heart attack [MedlinePlus Topic]
- melanocyte inducing transcription factor [ORDO Gene]
- melanocyte inducing transcription factor [HGNC gene]
- microbiology [MeSH Descriptor]
- microphthalmia-associated transcription factor [MeSH Descriptor]
HGNC gene
- melanocyte inducing transcription factor [HGNC gene]
NCIt concept(s)
- MITF Gene [NCIt concept]
- MITF wt Allele [NCIt concept]
- Microphthalmia-Associated Transcription Factor [NCIt concept]
ORDO concept(s)
- melanocyte inducing transcription factor [ORDO Gene]
Phenotypes related
- Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness [OMIM Phenotype]
- Melanoma, cutaneous malignant, susceptibility to, 8 [OMIM Phenotype]
- Tietz albinism-deafness syndrome [OMIM Phenotype]
- Waardenburg syndrome, type 2a [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- MITF Gene [NCIt concept]
- melanocyte inducing transcription factor [HGNC gene]

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