CORO1A, coronin 1A, 11151

N. diseases: 102; N. variants: 3
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: C3809383
Disease: IMMUNODEFICIENCY 8
IMMUNODEFICIENCY 8
disease Disease or Syndrome 1 3 0.700 strong 1.000 3 3 2009 2014
Severe combined immunodeficiency with low or normal B-cell numbers
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases Disease or Syndrome 2 0.200 None 1.000 1 2008 2008
CUI: C1270170
Disease: Disorder of chorion
Disorder of chorion
disease Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 3 0.010 None 1.000 1 2019 2019
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell Negative, B Cell Positive, NK Cell Positive
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases Disease or Syndrome 4 14 0.200 None 1.000 1 2008 2008
CUI: C0472817
Disease: WHIM syndrome
WHIM syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Infections; Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 10 7 0.010 None 1.000 1 2019 2019
CUI: C0851886
Disease: Pneumocystis Infections
Pneumocystis Infections
group Infections Disease or Syndrome 18 0.010 None 1.000 1 2018 2018
CUI: C2242635
Disease: Tumour thrombosis
Tumour thrombosis
disease Neoplastic Process 19 0.010 None 1.000 1 2013 2013
CUI: C0334529
Disease: Hydatidiform Mole, Partial
Hydatidiform Mole, Partial
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 20 0.100 None 0.900 10 2009 2020
Transfusion-Related Acute Lung Injury
disease Respiratory Tract Diseases; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 24 3 0.010 None 1.000 1 2019 2019
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 strong 1.000 1 2009 2009
X-Linked Combined Immunodeficiency Diseases
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases Disease or Syndrome 38 42 0.010 None 1.000 1 2019 2019
CUI: C0333693
Disease: Triploidy syndrome
Triploidy syndrome
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 42 0.020 None 1.000 2 2009 2011
CUI: C0220748
Disease: Cartilage-hair hypoplasia
Cartilage-hair hypoplasia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Immune System Diseases Disease or Syndrome; Congenital Abnormality 49 77 0.010 None 1.000 1 2019 2019
CUI: C0424166
Disease: Social Anxiety
Social Anxiety
disease Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 57 6 0.010 None 1.000 1 2014 2014
CUI: C0678213
Disease: Complete hydatidiform mole
Complete hydatidiform mole
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 61 3 0.100 None 1.000 13 2009 2020
CUI: C0014522
Disease: Epidermodysplasia Verruciformis
Epidermodysplasia Verruciformis
disease Infections; Skin and Connective Tissue Diseases Neoplastic Process 64 9 0.010 None 1.000 1 2014 2014
CUI: C3463897
Disease: HYDATIDIFORM MOLE, RECURRENT, 1
HYDATIDIFORM MOLE, RECURRENT, 1
disease Disease or Syndrome 66 14 0.040 None 1.000 4 2009 2019
CUI: C3272841
Disease: MUTYH-Associate Polyposis
MUTYH-Associate Polyposis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms Neoplastic Process 73 36 0.010 None 1.000 1 2018 2018
CUI: C0494261
Disease: Combined immunodeficiency
Combined immunodeficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases Disease or Syndrome 86 11 0.300 strong 1.000 1 2009 2009
CUI: C0398686
Disease: Primary immune deficiency disorder
Primary immune deficiency disorder
group Immune System Diseases Disease or Syndrome 93 23 0.010 None 1.000 1 2013 2013
CUI: C0004903
Disease: Beckwith-Wiedemann Syndrome
Beckwith-Wiedemann Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 107 84 0.030 None 1.000 3 2005 2019
CUI: C0020217
Disease: Hydatidiform Mole
Hydatidiform Mole
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 123 0.100 None 1.000 10 2009 2019
CUI: C1257925
Disease: Mammary Carcinoma, Animal
Mammary Carcinoma, Animal
disease Neoplasms; Animal Diseases Neoplastic Process 144 0.300 None 1.000 1 2011 2011
CUI: C0024667
Disease: Animal Mammary Neoplasms
Animal Mammary Neoplasms
phenotype Neoplasms; Animal Diseases Neoplastic Process 147 0.300 None 1.000 1 2011 2011
CUI: C1535939
Disease: Pneumocystis jiroveci pneumonia
Pneumocystis jiroveci pneumonia
disease Infections; Respiratory Tract Diseases Disease or Syndrome 180 5 0.010 None 1.000 1 2018 2018