Disease #01956 (CPTD1A (carnitine palmitoyltransferase deficiency, type IA), OMIM:255120)

Official abbreviation CPTD1A
Name carnitine palmitoyltransferase deficiency, type IA
OMIM ID 255120
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene CPT1A
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2024-11-14 14:49:30 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00181015 - - - - - - - - - - - CPTD1A - CPT1A CPT1A 1 1 Belen Perez
00301693 - - - M ? - - - - - - CPTD1A Cirrhosis CPT1A CPT1A 1 1 Ponghatai Boonsimma
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