GTP cyclohydrolase I deficiency

Summary

GTP cyclohydrolase I deficiency is a rare disease^[1].

Key Facts

• GTP cyclohydrolase I deficiency's instance of is recorded as rare disease^[2].
• GTP cyclohydrolase I deficiency's instance of is recorded as class of disease^[3].
• GTP cyclohydrolase I deficiency's subclass of is recorded as hyperphenylalaninemia^[4].
• GTP cyclohydrolase I deficiency's subclass of is recorded as enzymopathy^[5].
• GTP cyclohydrolase I deficiency's OMIM ID is recorded as 233910^[6].
• GTP cyclohydrolase I deficiency's Orphanet ID is recorded as 2102^[7].
• GTP cyclohydrolase I deficiency's NCI Thesaurus ID is recorded as C141442^[8].
• GTP cyclohydrolase I deficiency's genetic association is recorded as GCH1^[9].
• GTP cyclohydrolase I deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2102^[10].
• GTP cyclohydrolase I deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_238583^[11].
• GTP cyclohydrolase I deficiency's UMLS CUI is recorded as C0268467^[12].
• GTP cyclohydrolase I deficiency's UMLS CUI is recorded as C2673535^[13].
• GTP cyclohydrolase I deficiency's ICD-10-CM is recorded as E70.1^[14].
• GTP cyclohydrolase I deficiency's GARD rare disease ID is recorded as 2844^[15].
• GTP cyclohydrolase I deficiency's Mondo ID is recorded as MONDO_0009314^[16].
• GTP cyclohydrolase I deficiency's UniProt disease ID is recorded as DI-00538^[17].