DOID:9252	amino acid metabolic disorder
DOID:653	purine-pyrimidine metabolic disorder
DOID:906	peroxisomal disease
DOID:3146	lipid metabolism disorder
DOID:700	mitochondrial metabolism disease
DOID:3211	lysosomal storage disease
DOID:0050013	carbohydrate metabolism disease
DOID:870	neuropathy
DOID:1289	neurodegenerative disease
DOID:607	paraplegia
DOID:543	dystonia
DOID:1826	epilepsy
DOID:1443	cerebral degeneration
DOID:1561	cognitive disorder
DOID:0080006	bone development disease
DOID:2355	anemia
DOID:0050563	nonsyndromic deafness
DOID:5614	eye disease
DOID:37 	skin disease
DOID:557	kidney disease
DOID:3118	hepatobiliary disease
DOID:114	heart disease
DOID:423	myopathy
DOID:9120	amyloidosis
DOID:13268	porphyria
DOID:2914	immune system disease
DOID:162	cancer
DOID:0050177	monogenic disease
DOID:0050736	autosomal dominant disease
DOID:0050737	autosomal recessive disease