carnitine palmitoyltransferase I deficiency

Summary

carnitine palmitoyltransferase I deficiency is a rare disease^[1].

Key Facts

• carnitine palmitoyltransferase I deficiency's instance of is recorded as rare disease^[2].
• carnitine palmitoyltransferase I deficiency's instance of is recorded as class of disease^[3].
• carnitine palmitoyltransferase I deficiency is a type of lipid metabolism disorder^[4].
• carnitine palmitoyltransferase I deficiency is a type of disorder of carnitine cycle and carnitine transport^[5].
• carnitine palmitoyltransferase I deficiency is a type of genetic disease^[6].
• carnitine palmitoyltransferase I deficiency's ICD-9-CM is recorded as 277.85^[7].
• carnitine palmitoyltransferase I deficiency's NCI Thesaurus ID is recorded as C98871^[8].
• carnitine palmitoyltransferase I deficiency's genetic association is recorded as CPT1A^[9].
• carnitine palmitoyltransferase I deficiency's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0090129^[10].
• carnitine palmitoyltransferase I deficiency's exact match is recorded as http://identifiers.org/doid/DOID:0090129^[11].
• carnitine palmitoyltransferase I deficiency's on focus list of Wikimedia project is recorded as WikiProject Medicine^[12].