The following pages link to Griscelli syndrome type 2
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Albinism in humans (links | edit)
- Charcot–Marie–Tooth disease (links | edit)
- Melanin (links | edit)
- Joubert syndrome (links | edit)
- Freckle (links | edit)
- Vitiligo (links | edit)
- Argyria (links | edit)
- Lead poisoning (links | edit)
- Tietz syndrome (links | edit)
- Wolff–Parkinson–White syndrome (links | edit)
- Cardiofaciocutaneous syndrome (links | edit)
- Tuberous sclerosis (links | edit)
- Heterochromia iridum (links | edit)
- Waardenburg syndrome (links | edit)
- Melanism (links | edit)
- Acanthosis nigricans (links | edit)
- Noonan syndrome (links | edit)
- Li–Fraumeni syndrome (links | edit)
- Hyperpigmentation (links | edit)
- Hypopigmentation (links | edit)
- Peutz–Jeghers syndrome (links | edit)
- Incontinentia pigmenti (links | edit)
- CADASIL (links | edit)
- Café au lait spot (links | edit)
- Melasma (links | edit)
- Coffin–Lowry syndrome (links | edit)
- Neurofibromatosis type I (links | edit)
- Bardet–Biedl syndrome (links | edit)
- Leucism (links | edit)
- Chédiak–Higashi syndrome (links | edit)
- X-linked agammaglobulinemia (links | edit)
- Melanosis (links | edit)
- Chrysiasis (links | edit)
- Cowden syndrome (links | edit)
- Cherubism (links | edit)
- Neurofibromatosis type II (links | edit)
- Carpenter syndrome (links | edit)
- Metachondromatosis (links | edit)
- ABCD syndrome (links | edit)
- McCune–Albright syndrome (links | edit)
- Hermansky–Pudlak syndrome (links | edit)
- Oculocutaneous albinism (links | edit)
- Costello syndrome (links | edit)
- Lentigo (links | edit)
- ZAP70 deficiency (links | edit)
- List of ICD-9 codes 680–709: diseases of the skin and subcutaneous tissue (links | edit)
- Carney complex (links | edit)
- Bannayan–Riley–Ruvalcaba syndrome (links | edit)
- Liver spot (links | edit)
- Griscelli syndrome (links | edit)