CD3D, CD3d molecule, 915

N. diseases: 67; N. variants: 4
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: C3810147
Disease: IMMUNODEFICIENCY 19
IMMUNODEFICIENCY 19
disease Disease or Syndrome 1 3 0.610 strong 1.000 10 3 2003 2017
CUI: C1845609
Disease: Lymphoid depletion
Lymphoid depletion
disease Disease or Syndrome 4 0.010 None 1.000 1 1991 1991
CUI: C4025684
Disease: Recurrent abscess formation
Recurrent abscess formation
phenotype Finding 6 0.100 None 0
Failure to thrive secondary to recurrent infections
phenotype Finding 7 0.100 None 0
CUI: C4024599
Disease: Chronic oral candidiasis
Chronic oral candidiasis
disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 8 2 0.100 None 0
Decreased proportion of CD3-positive T cells
phenotype Immune System Diseases; Hemic and Lymphatic Diseases Finding 9 0.100 None 0
CUI: C1860128
Disease: Recurrent candida infections
Recurrent candida infections
phenotype Finding 12 1 0.100 None 0
Decreased lymphocyte proliferation in response to mitogen
phenotype Cell or Molecular Dysfunction 13 0.100 None 0
CUI: C1263762
Disease: Endocervical adenocarcinoma
Endocervical adenocarcinoma
disease Neoplastic Process 14 0.010 None 1.000 1 2019 2019
CUI: C1299237
Disease: Endocervical Carcinoma
Endocervical Carcinoma
disease Neoplastic Process 14 0.010 None 1.000 1 2019 2019
CUI: C0473133
Disease: Protracted diarrhea
Protracted diarrhea
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 14 0.100 None 0
CUI: C0242583
Disease: Bare Lymphocyte Syndrome
Bare Lymphocyte Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases Disease or Syndrome 24 0.300 None 1.000 1 2004 2004
CUI: C3532222
Disease: Inflammatory cardiomyopathy
Inflammatory cardiomyopathy
disease Cardiovascular Diseases Disease or Syndrome 25 0.010 None 1.000 1 2011 2011
CUI: C0151669
Disease: Increased antibody level in blood
Increased antibody level in blood
phenotype Finding 27 0.100 None 0
CUI: C0149504
Disease: Encephalopathy, Toxic
Encephalopathy, Toxic
disease Nervous System Diseases; Chemically-Induced Disorders Injury or Poisoning 29 0.300 None 1.000 1 2010 2010
CUI: C0154659
Disease: Toxic Encephalitis
Toxic Encephalitis
disease Nervous System Diseases; Chemically-Induced Disorders Injury or Poisoning 29 0.300 None 1.000 1 2010 2010
CUI: C0235032
Disease: Neurotoxicity Syndromes
Neurotoxicity Syndromes
group Nervous System Diseases; Chemically-Induced Disorders Injury or Poisoning 34 0.300 None 1.000 1 2010 2010
CUI: C2700553
Disease: Omenn Syndrome
Omenn Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases Disease or Syndrome 35 48 0.300 None 1.000 1 2004 2004
Acute monocytic/monoblastic leukemia
disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 35 2 0.010 None 1.000 1 1993 1993
CUI: C0238065
Disease: Secondary Biliary Cholangitis
Secondary Biliary Cholangitis
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 42 0.300 None 1.000 1 2008 2008
CUI: C4551595
Disease: Biliary Cirrhosis, Primary, 1
Biliary Cirrhosis, Primary, 1
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 42 0.300 None 1.000 1 2008 2008
CUI: C0694550
Disease: Recurrent pneumonia
Recurrent pneumonia
disease Infections; Respiratory Tract Diseases Finding 62 11 0.100 None 0
CUI: C0011606
Disease: Exfoliative dermatitis
Exfoliative dermatitis
disease Skin and Connective Tissue Diseases Disease or Syndrome 64 2 0.100 None 0
CUI: C0086565
Disease: Liver Dysfunction
Liver Dysfunction
phenotype Digestive System Diseases Finding 73 0.300 None 1.000 1 2010 2010
CUI: C0747085
Disease: Recurrent otitis media
Recurrent otitis media
disease Otorhinolaryngologic Diseases Disease or Syndrome 120 11 0.100 None 0