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Primary systemic amyloidosis
1 OMIM reference -
1 associated gene
66 connected diseases
No signs/symptoms info
Disease Type of connection
Apolipoprotein A-I deficiency
Familial renal amyloidosis due to Apolipoprotein AI variant
Epidermolytic palmoplantar keratoderma
Immunodeficiency due to an early component of complement deficiency
Cholesterol-ester transfer protein deficiency
Amyotrophic lateral sclerosis
Familial LCAT deficiency
Fish-eye disease
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
Familial amyloid polyneuropathy
Transthyretin-related familial amyloid cardiomyopathy
Tangier disease
Homozygous familial hypercholesterolemia
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16
Amyotrophic lateral sclerosis type 4
Annular epidermolytic ichthyosis
Autosomal dominant methemoglobinemia
Congenital analbuminemia
Corneal intraepithelial dyskeratosis with palmoplantar hyperkeratosis and laryngeal dyskeratosis
Dihydropteridine reductase deficiency
Epidermolytic ichthyosis
Familial afibrinogenemia
Familial dysfibrinogenemia
Familial hypodysfibrinogenemia
Familial hypofibrinogenemia
Familial renal amyloidosis due to fibrinogen A alpha-chain variant
Fibronectin glomerulopathy
Hb Bart's hydrops fetalis
Hemoglobin H disease
Horizontal gaze palsy with progressive scoliosis
Ichthyosis hystrix of Curth-Macklin
Keratosis palmoplantaris striata
Pachyonychia congenita
Recurrent infections associated with rare immunoglobulin isotypes deficiency
Spinocerebellar ataxia with axonal neuropathy type 2
Vitiligo-associated autoimmune disease
X-linked hyper-IgM syndrome
Xanthinuria type II
Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Familial renal amyloidosis due to Apolipoprotein AII variant
Adult-onset distal myopathy due to VCP mutation
Autosomal agammaglobulinemia
B-cell chronic lymphocytic leukemia
Behavioral variant of frontotemporal dementia
Congenital atransferrinemia
Familial partial lipodystrophy due to AKT2 mutations
Hereditary combined deficiency of vitamin K-dependent clotting factors
Hypoinsulinemic hypoglycemia and body hemihypertrophy
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Pediatric systemic lupus erythematosus
Progressive non-fluent aphasia
Semantic dementia
Spastic paraplegia - Paget disease of bone
Synpolydactyly type 2
T-B+ severe combined immunodeficiency due to JAK3 deficiency
Atypical hemolytic uremic syndrome with anti-factor H antibodies
C3 glomerulonephritis
Dense deposit disease
Congenital chronic diarrhea with protein-losing enteropathy
- Systemic AL amyloidosis
- Systemic immunoglobulinic amyloidosis

Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
- Rare hematologic disease
- Rare neurologic disease
- Rare oncologic disease
- Rare renal disease
- Rare systemic or rheumatologic disease

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

Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
APOA1 P02647107680
No signs/symptoms info available.