methylcobalamin deficiency type cblG
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methylcobalamin deficiency type cblG
Summary
methylcobalamin deficiency type cblG is a rare disease[1].
Key Facts
- methylcobalamin deficiency type cblG's instance of is recorded as rare disease[2].
- methylcobalamin deficiency type cblG's instance of is recorded as class of disease[3].
- methylcobalamin deficiency type cblG's subclass of is recorded as rare genetic renal disease[4].
- methylcobalamin deficiency type cblG's subclass of is recorded as thrombotic microangiopathy[5].
- methylcobalamin deficiency type cblG's OMIM ID is recorded as 250940[6].
- methylcobalamin deficiency type cblG's KEGG ID is recorded as H01285[7].
- methylcobalamin deficiency type cblG's Orphanet ID is recorded as 2170[8].
- methylcobalamin deficiency type cblG's genetic association is recorded as MTR[9].
- methylcobalamin deficiency type cblG's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2170[10].
- methylcobalamin deficiency type cblG's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_622[11].
- methylcobalamin deficiency type cblG's UMLS CUI is recorded as C1855128[12].
- methylcobalamin deficiency type cblG's ICD-10-CM is recorded as E72.1[13].
- methylcobalamin deficiency type cblG's GARD rare disease ID is recorded as 3577[14].
- methylcobalamin deficiency type cblG's Mondo ID is recorded as MONDO_0009609[15].
- methylcobalamin deficiency type cblG's UniProt disease ID is recorded as DI-01971[16].