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X-linked hyper-IgM syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Primary systemic amyloidosis
1 OMIM reference -
1 associated gene
No signs/symptoms info
X-linked hyper-IgM syndrome
Primary systemic amyloidosis

CD40LG
(UniProt - OMIM)
 APOA1
(UniProt - OMIM)

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
Primary systemic amyloidosis
APOA1



X-linked hyper-IgM syndrome
Primary systemic amyloidosis

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):
- Systemic AL amyloidosis
- Systemic immunoglobulinic amyloidosis
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
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):
- 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:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.