Classic congenital lipoid adrenal hyperplasia

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Classic congenital lipoid adrenal hyperplasia due to STAR deficency

ORPHA:325524Clinical subtype

Also called Classic CLAH

What it is

Orphanet has not published a description for this disease yet. The identifiers, classification and cross-references below are still current.

Key facts

Inheritance
Autosomal recessive
Classified as
Clinical subtype

Recorded for the broader condition

Age of onset
Childhood, Infancy, NeonatalCongenital lipoid adrenal hyperplasia due to STAR deficency

Orphanet records these for the broader condition rather than for this specific form. They are a starting point, not a figure for this subtype — subtypes often differ, and some are defined by being rarer than the condition they sit under.

Gene

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

ICD-10 codes

E25.0filed under a broader ICD-10 category — shared with 12 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.

Cross-references

MONDO 0017972UMLS C5679869

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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