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Familial amyloidosis, Finnish type
1 OMIM reference -
1 associated gene
38 connected diseases
No signs/symptoms info
Disease Type of connection
Baraitser-Winter syndrome
Childhood-onset nemaline myopathy
Congenital fiber-type disproportion myopathy
Congenital myopathy with excess of thin filaments
Intermediate nemaline myopathy
Severe congenital nemaline myopathy
Typical nemaline myopathy
Complete androgen insensitivity syndrome
Familial hypospadias
Kennedy disease
Partial androgen insensitivity syndrome
Fibronectin glomerulopathy
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Early-onset autosomal dominant Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Estrogen resistance syndrome
2p21 microdeletion syndrome
Familial isolated dilated cardiomyopathy
CLOVE syndrome
Congenital analbuminemia
Cowden syndrome
Dedifferentiated liposarcoma
Hereditary nonpolyposis colon cancer
Macrodactyly of fingers, unilateral
Megalencephaly-capillary malformation-polymicrogyria syndrome
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
Well-differentiated liposarcoma
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Giant cell glioblastoma
Developmental malformations - deafness - dystonia
Familial renal cell carcinoma
- Familial amyloid polyneuropathy type 4
- Gelsolin amyloidosis
- Hereditary amyloidosis, Finnish type

Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
GSN P06396137350
No signs/symptoms info available.