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Leukocyte adhesion deficiency type I
1 OMIM reference -
1 associated gene
12 connected diseases
No signs/symptoms info
Disease Type of connection
Chronic mucocutaneous candidiasis
Familial isolated dilated cardiomyopathy
Congenital high-molecular-weight kininogen deficiency
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Chronic myeloid leukemia
Precursor B-cell acute lymphoblastic leukemia
Precursor T-cell acute lymphoblastic leukemia
Autoimmune lymphoproliferative syndrome
Autosomal recessive systemic lupus erythematosus
Common variable immunodeficiency
Granulomatosis with polyangiitis
Spinocerebellar ataxia type 14
Synonym(s):
- LAD-I
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: childhood
Average age of death: before age 5
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
1 MeSH reference: C535887
Gene symbol UniProt reference OMIM reference
ITGB2 P05107600065
No signs/symptoms info available.