methylcobalamin deficiency type cblE

Summary

methylcobalamin deficiency type cblE is a rare disease^[1].

Key Facts

• methylcobalamin deficiency type cblE's instance of is recorded as rare disease^[2].
• methylcobalamin deficiency type cblE's instance of is recorded as class of disease^[3].
• methylcobalamin deficiency type cblE's subclass of is recorded as disease^[4].
• methylcobalamin deficiency type cblE's MeSH descriptor ID is recorded as C565510^[5].
• methylcobalamin deficiency type cblE's OMIM ID is recorded as 236270^[6].
• methylcobalamin deficiency type cblE's Orphanet ID is recorded as 2169^[7].
• methylcobalamin deficiency type cblE's genetic association is recorded as MTRR^[8].
• methylcobalamin deficiency type cblE's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2169^[9].
• methylcobalamin deficiency type cblE's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_622^[10].
• methylcobalamin deficiency type cblE's UMLS CUI is recorded as C1856057^[11].
• methylcobalamin deficiency type cblE's ICD-10-CM is recorded as E72.1^[12].
• methylcobalamin deficiency type cblE's Mondo ID is recorded as MONDO_0009354^[13].
• methylcobalamin deficiency type cblE's UniProt disease ID is recorded as DI-01970^[14].