glycinuria
human disease
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glycinuria
Summary
glycinuria is a hereditary disorder[1].
Key Facts
- glycinuria's instance of is recorded as hereditary disorder[2].
- glycinuria's subclass of is recorded as amino acid transport disorder[3].
- glycinuria's subclass of is recorded as genetic disease[4].
- glycinuria's MeSH descriptor ID is recorded as C563009[5].
- glycinuria's OMIM ID is recorded as 138500[6].
- glycinuria's KEGG ID is recorded as H01304[7].
- glycinuria's genetic association is recorded as SLC36A2[8].
- glycinuria's genetic association is recorded as SLC6A20[9].
- glycinuria's genetic association is recorded as SLC6A19[10].
- glycinuria's Google Knowledge Graph ID is recorded as /g/11vk8qx6h[11].
- glycinuria's exact match is recorded as http://purl.obolibrary.org/obo/HP_0003108[12].
- glycinuria's UMLS CUI is recorded as C0543541[13].
- glycinuria's UMLS CUI is recorded as C0341706[14].
- glycinuria's Human Phenotype Ontology ID is recorded as HP:0003108[15].
- glycinuria's Mondo ID is recorded as MONDO_0007677[16].
- glycinuria's UniProt disease ID is recorded as DI-02939[17].