Disease #01956

Official abbreviation -
Name carnitine palmitoyltransferase I deficiency
OMIM ID 255120
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene CPT1A
Associated tissues -
Disease features -
Remarks -


Individuals

1 entry on 1 page. Showing entry 1.
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00181015 - - - - - - - - - - - carnitine palmitoyltransferase I deficiency - CPT1A CPT1A 1 1 Maria Belen Perez Gonzalez
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