Kindler syndrome
Information
- Disease name
- Kindler syndrome
- Disease ID
- DOID:0060472
- Description
- "A skin disease characterized by congenital blistering, skin atrophy, photosensitivity, skin fragility, and scaling." [url:https\://en.wikipedia.org/wiki/Kindler_syndrome, url:https\://www.ncbi.nlm.nih.gov/pubmed/12668616]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT04908215 | Completed | Phase 2 | INM-755 (Cannabinol) Cream for Treatment of Epidermolysis Bullosa | December 28, 2021 | April 19, 2023 |
| NCT05033574 | Unknown status | The State of Sexual Development in Children With Inherited Epidermolysis Bullosa | December 8, 2020 | June 1, 2023 |
- Disase is a (Disease Ontology)
- DOID:37
- Cross Reference ID (Disease Ontology)
- GARD:4391
- Cross Reference ID (Disease Ontology)
- MESH:C536321
- Cross Reference ID (Disease Ontology)
- MIM:173650
- Cross Reference ID (Disease Ontology)
- ORDO:306539
- Exact Synonym (Disease Ontology)
- hereditary acrokeratotic poikiloderma of Kindler-Weary
- Exact Synonym (Disease Ontology)
- poikiloderma of Kindler
- OrphaNumber from OrphaNet (Orphanet)
- 2908