Disease #01955 (carnitine palmitoyltransferase II deficiency, late-onset, OMIM:255110)

Official abbreviation -
Name carnitine palmitoyltransferase II deficiency, late-onset
OMIM ID 255110
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene CPT2
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Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00095882 - - - - - - - - - - - carnitine palmitoyltransferase II deficiency, late-onset carnitine palmitoyl transferase II deficiency myopathic form (CPT2, adult-onset form); rhabdomyolysis (HP:0003201) CPT2 CPT2 1 1 Daniela Avila-Smirnow
00265254 - - - F - Spain - - - - - carnitine palmitoyltransferase II deficiency, late-onset - CPT2 CPT2 2 1 Jorge Docampo Cordeiro
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