Disorder of melanin metabolism
MONDO:001813415 clinical trials for this condition and its sub-types, 0 tagged with Disorder of melanin metabolism itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Disorder of melanin metabolism
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Syndromic oculocutaneous albinism 0 trials · 12 incl. sub-types
4 sub-types
- Chediak-Higashi syndrome 9 trials
- Hermansky-Pudlak syndrome 4 trials Sub-types →
- Griscelli syndrome 2 trials · 3 incl. sub-types Sub-types →
- Oculocerebral hypopigmentation syndrome, Cross type 0 trials
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Oculocutaneous albinism 4 trials
9 sub-types
- Oculocutaneous albinism type 1 0 trials · 1 incl. sub-types Sub-types →
- Autosomal dominant oculocutaneous albinism 0 trials
- Oculocutaneous albinism type 2 0 trials
- Oculocutaneous albinism type 3 0 trials
- Oculocutaneous albinism type 4 0 trials
- Oculocutaneous albinism type 5 0 trials
- Oculocutaneous albinism type 6 0 trials
- Oculocutaneous albinism type 7 0 trials
- Oculocutaneous albinism type 8 0 trials
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Ocular albinism 1 trial · 2 incl. sub-types
3 sub-types
- Autosomal recessive ocular albinism 0 trials · 1 incl. sub-types Sub-types →
- X-linked recessive ocular albinism 0 trials
- Ocular albinism with late-onset sensorineural deafness 0 trials
Most studied deeper sub-types
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New drug combo shows promise for kids with rare immune disease
Disease control CompletedThis study tested a drug called alemtuzumab (Campath) as a first treatment for children with hemophagocytic lymphohistiocytosis (HLH), a rare and life-threatening immune disorder. The goal was to see if it could help children survive until they could receive a stem cell transplan…
Phase 1/2 • Sponsor: Assistance Publique - Hôpitaux de Paris • Aim: Disease control
Last updated Jun 27, 2026 12:02 UTC
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Hunting for hidden genes behind albinism
Knowledge-focused CompletedThis study investigates people with oculocutaneous albinism who have no known genetic cause for their condition. Researchers use advanced DNA analysis techniques to search for new or hidden mutations. The goal is to improve diagnosis and understanding of this inherited condition.
Sponsor: University Hospital, Bordeaux • Aim: Knowledge-focused
Last updated Jun 27, 2026 14:00 UTC