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Familial primary localized cutaneous amyloidosis
2 OMIM references -
2 associated genes
6 connected diseases
No signs/symptoms info
Disease Type of connection
Stüve-Wiedemann syndrome
Budd-Chiari syndrome
Essential thrombocythemia
Familial thrombocytosis
Myelofibrosis with myeloid metaplasia
Polycythemia vera
Synonym(s):
- FPLCA
Classification (Orphanet):
- Rare genetic disease
- Rare skin disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
External references:
2 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
IL31RA Q8NI17609510
OSMR Q99650601743
No signs/symptoms info available.