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LAMB-2-related infantile-onset nephrotic syndrome
1 OMIM reference -
1 associated gene
20 connected diseases
No signs/symptoms info
Disease Type of connection
Pierson syndrome
Synaptic congenital myasthenic syndromes
Acute myeloblastic leukemia with maturation
Acute myeloblastic leukemia without maturation
Acute myelomonocytic leukemia
Acute promyelocytic leukemia
Atypical Gaucher disease due to saposin C deficiency
Autosomal dominant hyper-IgE syndrome
Encephalopathy due to prosaposin deficiency
Infantile Krabbe disease
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus
Metachromatic leukodystrophy, adult form
Metachromatic leukodystrophy, juvenile form
Metachromatic leukodystrophy, late infantile form
Spinocerebellar ataxia type 7
Congenital muscular dystrophy type 1A
Familial isolated dilated cardiomyopathy
Generalized junctional epidermolysis bullosa, non-Herlitz type
Junctional epidermolysis bullosa, Herlitz type
LOC syndrome
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Diseases of the genitourinary system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
LAMB2 P55268150325
No signs/symptoms info available.