Fetal hemoglobin quantitative trait locus 6

Preferred Label : Fetal hemoglobin quantitative trait locus 6;

Symbol : HBFQTL6;

CISMeF acronym : HBFQTL6;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Hereditary persistence of fetal hemoglobin, klf1-related;

Prefixed ID : #613566;

Details

Origin ID

613566;

UMLS CUI

C3150805;

Automatic exact mappings (from CISMeF team)
- Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome [ORDO Disease]
- KLF1 wt Allele [NCIt concept]
Genes related to phenotype
- Kruppel-like factor 1 [OMIM gene]
ORDO concept(s)
- Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome [ORDO Disease]
- Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome [ORDO Disease]
See also inter- (CISMeF)
- Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome [ORDO Disease]
- Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome [ORDO Disease]
Semantic type(s)
- Finding [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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