
Glycogen Storage Disease (Type I、
II)
Hepatolenticular
Degeneration(Wilson Disease)
Hereditary Angioedema (HAE)
Hereditary Epidermolysis Bullosa
Hereditary Fructose Intolerance
Hereditary Hypomagnesemia
Hereditary Multi-infarct Dementia
(Cerebral Autosomal Dominant
Arteriopathy with Subcortical
Infarcts and Leukoencephalopathy,
CADASIL)
Hereditary Spastic Paraplegia
Holocarboxylase Synthetase
Deficiency