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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Atypical Gaucher disease due to saposin C deficiency
LAMB-2-related infantile-onset nephrotic syndrome

PSAP LAMB2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PSAP
(0.63)
LAMB2



Citations in the biomedical literature:


Atypical Gaucher disease due to saposin C deficiency
PSAP
LAMB-2-related infantile-onset nephrotic syndrome
LAMB2



Atypical Gaucher disease due to saposin C deficiency
LAMB-2-related infantile-onset nephrotic syndrome

Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Diseases of the genitourinary system -

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

No signs/symptoms info available.