Carnitine palmitoyl transferase 1A…

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Carnitine palmitoyl transferase 1A deficiency

ORPHA:156Disease

Also called CPT1A deficiency · Carnitine palmitoyl transferase IA deficiency · Hepatic carnitine palmitoyl transferase 1 deficiency · Hepatic carnitine palmitoyl transferase I deficiency · L-CPT1 deficiency · L-CPTI deficiency

What it is

Carnitine palmitoyltransferase 1A (CPT-1A) deficiency is an inborn error of metabolism that affects mitochondrial oxidation of long chain fatty acids (LCFA) in the liver and kidneys, and is characterized by recurrent attacks of fasting-induced hypoketotic hypoglycemia and risk of liver failure.

Key facts

Prevalence
<1 / 1 000 000
Age of onset
Infancy, Neonatal
Inheritance
Autosomal recessive
Classified as
Disease

Prevalence figures describe populations, not individuals, and are often estimates from a single study. Where the figure is an incidence or a birth prevalence, it says so.

Signs and symptoms

These ranges are how often a sign appears across everyone diagnosed, not a prediction for one person — most people have some of these and not others. Orphanet also records findings that are specifically absent in this disease; those are in the data but not listed here.

Gene

CPT1ADisease-causing germline mutation(s) (loss of function)

ICD-10 codes

E71.3filed under a broader ICD-10 category — shared with 27 other rare diseases

ICD-10 has no distinct code for most rare diseases, so many are filed under the nearest available one. A shared code identifies the group, not this disease — the ORPHAcode above is what identifies it.

Related health topics

Reached through the ICD-10 categories this disease is filed under, so these describe the broader group rather than this disease specifically.

Cross-references

GARD 1120MESH C535588MONDO 0009705OMIM 255120UMLS C1829703

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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