citrin deficiency
monogenetic inherited metabolic disease
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citrin deficiency
Summary
citrin deficiency is a class of disease[1]. It draws 6 Wikipedia views per month (class_of_disease category, ranking #627 of 1,968).[2]
Key Facts
- citrin deficiency's instance of is recorded as class of disease[3].
- citrin deficiency's subclass of is recorded as citrullinemia[4].
- citrin deficiency's Orphanet ID is recorded as 247582[5].
- citrin deficiency's genetic association is recorded as SLC25A13[6].
- citrin deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_247582[7].
- citrin deficiency's UMLS CUI is recorded as C1863844[8].
- citrin deficiency's UMLS CUI is recorded as C1997910[9].
- citrin deficiency's ICD-10-CM is recorded as E72.2[10].
- citrin deficiency's Mondo ID is recorded as MONDO_0016602[11].
- citrin deficiency's ICD-11 ID is recorded as 348535193[12].
Why It Matters
citrin deficiency draws 6 Wikipedia views per month (class_of_disease category, ranking #627 of 1,968).[2]