21695-2LOINC 2.82
HFE gene.p.Cys282Tyr [Presence] in Blood or Tissue by Molecular genetics method
HFE p.C282Y Bld/T Ql
Definition
- Dominant cause of hemochromatosis (>90% cases) at least in US
Component
- HFE gene.p.Cys282Tyr
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- PrThr
Scale
- Ord
Method
- Molgen
Related names
- 845G>A; Blood; Cys282Tyr; Genetics; Haemochromatosis; hemochromatosis; Hereditary hemochromatosis; Heredity; Heritable; HFE p.C282Y; HFE1; HH; HLAH; HLA-H; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; MVCD7; Ordinal; P prime; PCR; Point in time; PR; QL; Qual; Qualitative; Random; Screen; TFQTL2; Tissue; Tissue, unspecified; UniversalLabOrders; WB; Whole blood; Whole blood or Tissue
Index terms
- 845G>
- A
- Blood
- Cys282Tyr
- Genetics
- Haemochromatosis
- hemochromatosis
- Hereditary hemochromatosis
- Heredity
- Heritable
- HFE p.C282Y
- HFE1
- HH
- HLA-H
- HLAH
- Inherited
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- MVCD7
- Ordinal
- P prime
- PCR
- Point in time
- PR
- QL
- Qual
- Qualitative
- Random
- Screen
- TFQTL2
- Tissue
- Tissue, unspecified
- UniversalLabOrders
- WB
- Whole blood
- Whole blood or Tissue