URI(s)
- http://id.loc.gov/authorities/subjects/sh85084017
- http://id.loc.gov/authorities/sh85084017#concept
Variants
- Hereditary metabolic disorders
- Inborn errors of metabolism
Broader Terms
Narrower Terms
- Achondroplasia
- Adenosine deaminase deficiency
- Chronic granulomatous disease
- Galactosemias
- Glucose-6-phosphate dehydrogenase deficiency
- Glycogen storage disease
- Gout
- Hemochromatosis
- Hypophosphatemia, Familial
- Lesch-Nyhan syndrome
- Lysosomal storage diseases
- Neuronal ceroid-lipofuscinoses
- Ornithine carbamoyltransferase deficiency
- Peroxisomal disorders
- Phenylketonurias
Closely Matching Concepts from Other Schemes
Broader Concepts from Other Schemes
LC Classification
- RC627.8
Instance Of
Scheme Membership(s)
Collection Membership(s)
Change Notes
- 1986-02-11: new
- 1987-05-04: revised
Alternate Formats
