CASP10, caspase 10, 843

N. diseases: 166; N. variants: 16
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C1858968
Disease: Autoimmune Lymphoproliferative Syndrome, Type IIA
Autoimmune Lymphoproliferative Syndrome, Type IIA 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 1 1 0.730 strong 1.000 4 1 1999 2011
CUI: C4703376
Disease: Increased proportion of HLA DR+ T cells
Increased proportion of HLA DR+ T cells 		phenotype Finding 3 0.100 None 0
CUI: C0241185
Disease: Smooth muscle antibodies positive
Smooth muscle antibodies positive 		phenotype Laboratory or Test Result 4 0.100 None 0
CUI: C1843386
Disease: Reduced delayed hypersensitivity
Reduced delayed hypersensitivity 		phenotype Finding 4 0.100 None 0
CUI: C1858980
Disease: Platelet antibody positive
Platelet antibody positive 		phenotype Laboratory or Test Result 4 0.100 None 0
CUI: C1858969
Disease: Decreased lymphocyte apoptosis
Decreased lymphocyte apoptosis 		phenotype Finding 5 0.100 None 0
CUI: C1858972
Disease: Increased B cell count
Increased B cell count 		phenotype Hemic and Lymphatic Diseases Finding 5 0.100 None 0
CUI: C1858973
Disease: Elevated proportion of CD4-negative, CD8-negative, alpha-beta regulatory T cells
Elevated proportion of CD4-negative, CD8-negative, alpha-beta regulatory T cells 		phenotype Finding 5 0.100 None 0
CUI: C4021032
Disease: Abnormal vitamin B12 level
Abnormal vitamin B12 level 		phenotype Finding 5 0.100 None 0
CUI: C4531156
Disease: Abnormal proportion of CD4 T cells
Abnormal proportion of CD4 T cells 		phenotype Finding 5 0.100 None 0
CUI: C0520736
Disease: Coombs positive hemolytic anemia
Coombs positive hemolytic anemia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 6 0.100 None 0
CUI: C2674723
Disease: RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER
RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 6 14 0.100 None 0 2
CUI: C4021747
Disease: Specific anti-polysaccharide antibody deficiency
Specific anti-polysaccharide antibody deficiency 		phenotype Finding 6 0.100 None 0
CUI: C4280772
Disease: Abnormal serum interleukin level
Abnormal serum interleukin level 		phenotype Finding 6 0.100 None 0
CUI: C4531155
Disease: Abnormal proportion of CD8 T cells
Abnormal proportion of CD8 T cells 		phenotype Finding 6 0.100 None 0
CUI: C0151379
Disease: Rheumatoid factor positive (finding)
Rheumatoid factor positive (finding) 		phenotype Laboratory or Test Result 7 0.100 None 0
CUI: C0178421
Disease: Fibroadenoma of breast
Fibroadenoma of breast 		disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 11 0.100 None 0
CUI: C4014733
Disease: Follicular hyperplasia
Follicular hyperplasia 		phenotype Hemic and Lymphatic Diseases Finding 11 0.100 None 0
CUI: C1858970
Disease: Chronic noninfectious lymphadenopathy
Chronic noninfectious lymphadenopathy 		phenotype Hemic and Lymphatic Diseases Finding 12 0.100 None 0
CUI: C0277942
Disease: Butterfly rash
Butterfly rash 		phenotype Skin and Connective Tissue Diseases Finding 13 0.100 None 0
CUI: C1846545
Disease: Autoimmune Lymphoproliferative Syndrome Type 2B
Autoimmune Lymphoproliferative Syndrome Type 2B 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 14 2 0.020 None 1.000 2 2003 2009
CUI: C4703633
Disease: Increased level of L-fucose in urine
Increased level of L-fucose in urine 		phenotype Finding 14 0.100 None 0
CUI: C1858981
Disease: Antineutrophil antibody positivity
Antineutrophil antibody positivity 		phenotype Laboratory or Test Result 15 0.100 None 0
CUI: C0153943
Disease: Benign neoplasm of stomach
Benign neoplasm of stomach 		disease Digestive System Diseases; Neoplasms Neoplastic Process 17 0.300 None 0
CUI: C0496905
Disease: Neoplasm of uncertain or unknown behavior of stomach
Neoplasm of uncertain or unknown behavior of stomach 		disease Digestive System Diseases; Neoplasms Neoplastic Process 17 0.300 None 0