peeling skin syndrome
Information
- Disease name
- peeling skin syndrome
- Disease ID
- DOID:0060283
- Description
- "A skin disease that is characterized by the painless, continuous peeling of the top layer of skin." [url:https\://rarediseases.org/rare-diseases/peeling-skin-syndrome/]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:37
- Cross Reference ID (Disease Ontology)
- GARD:7347
- Cross Reference ID (Disease Ontology)
- MESH:C564818
- Cross Reference ID (Disease Ontology)
- MIM:PS270300
- Cross Reference ID (Disease Ontology)
- ORDO:817
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:724838009
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C1849193
- Exact Synonym (Disease Ontology)
- deciduous skin
- Exact Synonym (Disease Ontology)
- familial continuous skin peeling syndrome
- Exact Synonym (Disease Ontology)
- keratosis exfoliativa congenita
- Exact Synonym (Disease Ontology)
- peeling skin disease
- OMIM Phenotype Series Number (OMIM)
- PS270300
- OrphaNumber from OrphaNet (Orphanet)
- 817
- MedGen concept unique identifier (MedGen Concept name)
- C1849193
- MedGen unique identifier (MedGen Concept name)
- 336530