|
PAS | Major components and autoantigen targets | Minor components and autoantigen targets | Genetic |
|
I | Addison’s disease | 21-Hydroxylase | Gonadal failure | P450 side-chain cleavage enzyme, 17a-hydroxylase | AIRE gene mutations (chromosome 21) |
Chronic hypoparathyroidism Chronic candidiasis (at least 2 present) | Calcium-sensing receptor | Vitiligo | SOX9, SOX10, tyrosinase |
| | | Alopecia | Tyrosine hydroxylase | |
II | Addison’s disease (always present) | 21-Hydroxylase | Atrophic gastritis | H+/K+ pump ATPase | Polygenic inheritance (HLA-DR3, chromosome 6) |
| | Pernicious anaemia | Intrinsic factor |
Thyroid autoimmune diseases | TSH-receptor Thyroid peroxidase Thyroglobulin | Celiac disease | Transglutaminase |
| | Autoimmune hepatitis | P450 (IID6, IA2) |
Type 1 diabetes mellitus | Glutamic acid decarboxylase Tyrosine-phosphatase Insulin | Hypophysitis and so forth | 68, 49, 43 kD from human |
III | Thyroid autoimmune diseases associated with endocrinopathy other than Addison’s disease | TSH-receptor Thyroid peroxidase Thyroglobulin | Celiac disease | Transglutaminase | Polygenic inheritance (HLA-DR3, chromosome 6) |
Autoimmune hepatitis | P450 (IID6, IA2) |
Myasthenia gravis and so forth | Acetylcholine receptor |
IIIA | Autoimmune thyroiditis | Thyroid peroxidase | | |
Type 1 diabetes mellitus | Glutamic acid decarboxylase Tyrosine-phosphatase Insulin | | |
IIIB | Autoimmune thyroiditis | Thyroid peroxidase | | |
Pernicious anaemia | Intrinsic factor | | |
IIIC | Autoimmune thyroiditis | Thyroid peroxidase | | |
Vitiligo | SOX9, SOX10, tyrosinase | | |
Alopecia | Tyrosine hydroxylase | | |
Other organ-specific autoimmune disease | | |
IV | Combination of organ-specific autoimmune diseases that do not fall in the previous types | | Gonadal failure | P450 side-chain cleavage enzyme, 17a-hydroxylase | Polygenic inheritance (HLA-DR3, chromosome 6) |
| Vitiligo | SOX9, SOX10, tyrosinase |
| Alopecia | Tyrosine hydroxylase |
| Atrophic gastritis | H+/K+ pump ATPase |
| Pernicious anaemia | Intrinsic factor |
| Celiac disease | Transglutaminase |
| Autoimmune hepatitis | P450 (IID6, IA2) |
| Hypophysitis and so forth | 68, 49, 43 kD from human |
|