HRAS, HRas proto-oncogene, GTPase, 3265

N. diseases: 71; N. variants: 21
Source: CLINVAR ×
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.
Squamous cell carcinoma of the head and neck
disease Neoplasms Neoplastic Process 27 179 0.150 None 1.000 1 6 1990 2018
CUI: C0040100
Disease: Thymoma
Thymoma
disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 2 9 0.140 None 1.000 2 1 2009 2017
CUI: C0553723
Disease: Squamous cell carcinoma of skin
Squamous cell carcinoma of skin
disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 12 54 0.130 None 1.000 4 6 1988 2016
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Neoplastic Process 15 76 0.130 None 1.000 1 8 1990 2016
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
MYELODYSPLASTIC SYNDROME
group Hemic and Lymphatic Diseases Neoplastic Process 11 19 0.130 None 1.000 1 2 1988 2016
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma
disease Digestive System Diseases; Neoplasms Neoplastic Process 16 102 0.130 None 1.000 1 2 1992 2016
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
disease Neoplasms Neoplastic Process 22 115 0.130 None 1.000 1 2 1987 2016
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy
disease Cardiovascular Diseases Disease or Syndrome 29 468 0.120 None 1.000 9 1 2005 2017
CUI: C0281361
Disease: Adenocarcinoma of pancreas
Adenocarcinoma of pancreas
disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 18 114 0.120 None 1.000 1 6 1994 2016
CUI: C0557874
Disease: Global developmental delay
Global developmental delay
disease Mental or Behavioral Dysfunction 303 505 0.120 None 1.000 1 1 2005 2017
Transitional cell carcinoma of bladder
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Neoplastic Process 26 141 0.110 None 1.000 1 7 1998 2016
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 11 51 0.110 None 1.000 1 4 1991 2016
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung
disease Neoplasms; Respiratory Tract Diseases Neoplastic Process 22 135 0.110 None 1.000 1 5 1985 2016
CUI: C0334517
Disease: Spermatocytic seminoma
Spermatocytic seminoma
disease Neoplasms; Male Urogenital Diseases; Endocrine System Diseases Neoplastic Process 2 2 0.110 None 1.000 0 1 2013 2013
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 237 350 0.100 None 1.000 10 1 2002 2017
CUI: C1845847
Disease: Coarse facial features
Coarse facial features
phenotype Pathological Conditions, Signs and Symptoms Finding 20 33 0.100 None 1.000 9 1 2005 2009
CUI: C1956257
Disease: Pulmonary Stenosis
Pulmonary Stenosis
disease Cardiovascular Diseases Disease or Syndrome 19 38 0.100 None 1.000 9 1 2005 2009
CUI: C1857539
Disease: Deep palmar crease
Deep palmar crease
phenotype Finding 7 8 0.100 None 1.000 9 1 2005 2009
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus
disease Nervous System Diseases Disease or Syndrome 22 24 0.100 None 1.000 9 1 2005 2009
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
disease Musculoskeletal Diseases Disease or Syndrome 63 92 0.100 None 1.000 9 1 2005 2009
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure
disease Cardiovascular Diseases Disease or Syndrome 8 9 0.100 None 1.000 9 1 2005 2009
CUI: C3714796
Disease: Isolated somatotropin deficiency
Isolated somatotropin deficiency
disease Disease or Syndrome 12 12 0.100 None 1.000 9 1 2005 2009
CUI: C0238441
Disease: Subglottic stenosis
Subglottic stenosis
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases Anatomical Abnormality 2 2 0.100 None 1.000 9 1 2005 2009
CUI: C3808548
Disease: Poor respiratory effort
Poor respiratory effort
phenotype Finding 1 1 0.100 None 1.000 5 1 2006 2012
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 336 579 0.100 None 1.000 5 1 2006 2012