Name: Familial hypercholesterolemia (disorder)
See more descriptions.
- Familial hypercholesterolemia (disorder)
- Familial hypercholesterolaemia
- Familial hypercholesterolemia
- Familial hyperbetalipoproteinaemia
- Essential familial hypercholesterolaemia
- Essential familial hypercholesterolemia
- Familial hyperbetalipoproteinemia
- LDL receptor disorder
- LDL - Low density lipoprotein receptor disorder
- Low density lipoprotein catabolic defect
Hide descriptions.
Concept ID: 398036000- Familial hypercholesterolaemia
- Familial hypercholesterolemia
- Familial hyperbetalipoproteinaemia
- Essential familial hypercholesterolaemia
- Essential familial hypercholesterolemia
- Familial hyperbetalipoproteinemia
- LDL receptor disorder
- LDL - Low density lipoprotein receptor disorder
- Low density lipoprotein catabolic defect
Hide descriptions.
Read Codes: C3200
ICD-10 Codes: E782 E780 Z713
- Familial hypercholesterolaemia due to genetic defect of apolipoprotein B
- Familial hypercholesterolaemia due to heterozygous LDL receptor mutation
- Familial hypercholesterolemia - heterozygous (disorder)
- Familial hypercholesterolemia - homozygous (disorder)
- Familial hypercholesterolemia co-occurrent and due to combined heterozygous low density lipoprotein receptor and low density lipoprotein receptor adaptor protein 1 mutations (disorder)
- Familial hypercholesterolemia due to homozygous low density lipoprotein receptor mutation (disorder)
- Fredrickson type IIa hyperlipoproteinemia (disorder)