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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
X-linked hyper-IgM syndrome
Familial renal amyloidosis due to Apolipoprotein AI variant

CD40LG APOA1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CD40LG
(0.72)
APOA1



Citations in the biomedical literature:


X-linked hyper-IgM syndrome
CD40LG
Familial renal amyloidosis due to Apolipoprotein AI variant
APOA1



X-linked hyper-IgM syndrome
Familial renal amyloidosis due to Apolipoprotein AI variant

Synonym(s):
- HIGM1
- Hyper-IgM syndrome due to CD40 ligand deficiency
- Hyper-IgM syndrome due to CD40L deficiency
- Hyper-IgM syndrome type 1
- XHIGM

Synonym(s):
- Apolipoprotein AI amyloidosis
- Familial amyloid nephropathy due to apolipoprotein AI variant
- Hereditary amyloid nephropathy due to apolipoprotein AI variant
- Hereditary renal amyloidosis due to apolipoprotein AI variant

Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease

Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.