Cytoscape Web
Click node...

Hepatic veno-occlusive disease - immunodeficiency
1 OMIM reference -
1 associated gene
11 connected diseases
No signs/symptoms info
Disease Type of connection
Acute myeloid leukemia with CEBPA somatic mutations
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Familial amyloid polyneuropathy
Inherited acute myeloid leukemia
Isolated NADH-CoQ reductase deficiency
Multiple endocrine neoplasia type 1
Proximal spinal muscular atrophy type 1
Proximal spinal muscular atrophy type 2
Proximal spinal muscular atrophy type 3
Proximal spinal muscular atrophy type 4
Transthyretin-related familial amyloid cardiomyopathy
Synonym(s):
- VODI syndrome
Classification (Orphanet):
- Rare genetic disease
- Rare hepatic disease
- Rare immune disease
Classification (ICD10):
- Diseases of the digestive system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
SP110 Q9HB58604457
No signs/symptoms info available.