Griscelli Syndrome Type 1 C1859194
A rare genetic condition affecting skin color and nervous system development due to melanin transport defects. It causes silvery hair, hypopigmentation, and neurological problems. Care focuses on symptom management.
Key facts at a glance
- ICD-10
- G40.909
- ICD-11
- 8A00.0
- Body system
- neurologic
- Severity
- severe
- Chronic
- true
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 25, 2026. · Read our editorial policy