377794 group of disorders
98053 Rare genetic disease
|
|
68367 Rare inborn errors of metabolism
|
137 Congenital disorder of glycosylation
4
309005 Disorder of lipid metabolism
4
309340 Disorder of lysosomal-related organelles
309813 Disorder of porphyrin and haem metabolism
2
309824 Disorder of metabolite absorption and transport
2
68366 Lysosomal disease
7
68373 Peroxisomal disease
3
79062 Disorder of amino acid and other organic acid metabolism
17
79161 Disorder of carbohydrate metabolism
9
79200 Disorder of energy metabolism
5
79214 Disorder of biogenic amine metabolism and transport
4
79224 Disorder of purine or pyrimidine metabolism
2
91088 Other metabolic disease