This is just here as a test because I lose it
Term information
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disease has basis in
- mitochondrial complex V (ATP synthase) deficiency nuclear type 2
- mitochondrial complex V (ATP synthase) deficiency nuclear type 3
- mitochondrial complex V (ATP synthase) deficiency nuclear type 4
- glycerol kinase deficiency
- mitochondrial complex III deficiency nuclear type 2
- chylomicron retention disease
- multiple acyl-CoA dehydrogenase deficiency
- acrodermatitis enteropathica
- primary cutaneous amyloidosis
- Gaucher's disease type II
- Gaucher's disease type I
- atypical Gaucher's disease due to saposin c deficiency
- Gaucher's disease perinatal lethal
- mitochondrial complex V (ATP synthase) deficiency nuclear type 1
- deafness-dystonia-optic neuronopathy syndrome
- mevalonic aciduria
- aspartylglucosaminuria
- Axenfeld-Rieger syndrome type 3
- Axenfeld-Rieger syndrome type 1
- maturity-onset diabetes of the young type 1
- congenital bile acid synthesis defect 3
- congenital bile acid synthesis defect 2
- congenital bile acid synthesis defect 4
- congenital bile acid synthesis defect 6
- congenital bile acid synthesis defect 5
- congenital bile acid synthesis defect 1
- glycogen storage disease IXb
- hemochromatosis type 2A
- hemochromatosis type 1
- hemochromatosis type 4
- hemochromatosis type 3
- hemochromatosis type 2B
- hemochromatosis type 5
- cerebral amyloid angiopathy
- maturity-onset diabetes of the young type 11
- maturity-onset diabetes of the young type 3
- maturity-onset diabetes of the young type 5
- maturity-onset diabetes of the young type 6
- maturity-onset diabetes of the young type 4
- maturity-onset diabetes of the young type 7
- maturity-onset diabetes of the young type 10
- maturity-onset diabetes of the young type 9
- maturity-onset diabetes of the young type 2
- mitochondrial complex II deficiency
- lysinuric protein intolerance
- Niemann-Pick disease type A
- Niemann-Pick disease type C2
- Niemann-Pick disease type B
- Niemann-Pick disease type C1
- methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
- methylmalonic acidemia due to transcobalamin receptor defect
- methylmalonic acidemia cblA type
- methylmalonic acidemia cblB type
- ethylmalonic encephalopathy
- apparent mineralocorticoid excess syndrome
- primary coenzyme Q10 deficiency 5
- primary coenzyme Q10 deficiency 6
- primary coenzyme Q10 deficiency 3
- primary coenzyme Q10 deficiency 4
- primary coenzyme Q10 deficiency 7
- primary coenzyme Q10 deficiency 8
- primary coenzyme Q10 deficiency 2
- primary coenzyme Q10 deficiency 1
- mitochondrial complex III deficiency nuclear type 6
- mitochondrial complex III deficiency nuclear type 7
- mitochondrial complex III deficiency nuclear type 8
- mitochondrial complex III deficiency nuclear type 9
- mitochondrial complex III deficiency nuclear type 1
- mitochondrial complex III deficiency nuclear type 3
- mitochondrial complex III deficiency nuclear type 4
- mitochondrial complex III deficiency nuclear type 5
- dopamine beta-hydroxylase deficiency
- D-bifunctional protein deficiency
- familial isolated deficiency of vitamin E
- aromatic L-amino acid decarboxylase deficiency
- carnitine palmitoyltransferase I deficiency
- lethal congenital glycogen storage disease of heart
- autosomal recessive hypercholesterolemia
- immunoglobulin light chain amyloidosis
- molybdenum cofactor deficiency type C
- molybdenum cofactor deficiency type B
- molybdenum cofactor deficiency type A
- maturity-onset diabetes of the young type 13
- maturity-onset diabetes of the young type 14