I-PORPHYRIA, HEPATIC AND ERYTHROPOIETIC (PORPHYRIN)
A-Early mitochondrial:
1-ALAD porphyria
2-Acute intermittent porphyria
B-Cytoplasmic:
1-Gunther disease/congenital erythropoietic porphyria
2-Porphyria cutanea tarda/Hepatoerythropoietic porphyria
C-Late mitochondrial:
1-Hereditary coproporphyria
2-Harderoporphyria
3-Variegate porphyria
4-Erythropoietic protoporphyria
II-HEREDITARY HYPERBILIRUBINEMIA (BILIRUBIN)
A-Unconjugated:
1-Gilbert’s syndrome
2-Crigler–Najjar syndrome
3-Lucey–Driscoll syndrome
B-Conjugated:
1-Dubin–Johnson syndrome
2-Rotor syndrome
