DLC1, DLC1 Rho GTPase activating protein, 10395

N. diseases: 144; N. variants: 21
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: C0086664
Disease: Myelocele
Myelocele
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality 5 1 0.100 None 0 1
NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO
disease Finding 11 30 0.100 None 0 2
CUI: C0155826
Disease: Chronic nasopharyngitis
Chronic nasopharyngitis
disease Infections; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 12 0.010 None 1.000 1 2014 2014
CUI: C4727070
Disease: Advanced Carcinoma
Advanced Carcinoma
disease Neoplastic Process 15 0.010 None 1.000 1 2009 2009
CUI: C0037383
Disease: Sneezing
Sneezing
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 21 2 0.010 None 1.000 1 2015 2015
Supratentorial Embryonal Tumor, Not Otherwise Specified
disease Neoplasms; Nervous System Diseases Neoplastic Process 22 4 0.010 None 1.000 1 2005 2005
Hereditary nonpolyposis colorectal carcinoma
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nutritional and Metabolic Diseases Neoplastic Process 28 5 0.100 None 0
CUI: C0020492
Disease: Hyperostosis
Hyperostosis
disease Musculoskeletal Diseases Disease or Syndrome 50 3 0.010 None 1.000 1 2017 2017
CUI: C0280631
Disease: Leiomyosarcoma of uterus
Leiomyosarcoma of uterus
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 71 0.100 None 0
CUI: C0080174
Disease: Spina Bifida Occulta
Spina Bifida Occulta
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality 76 6 0.100 None 0 1
CUI: C0030186
Disease: Paget Disease Extramammary
Paget Disease Extramammary
disease Neoplasms Neoplastic Process 79 1 0.010 None 1.000 1 2012 2012
CUI: C0025312
Disease: Meningomyelocele
Meningomyelocele
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality 89 27 0.100 None 0 2
CUI: C0034885
Disease: Rectal Neoplasms
Rectal Neoplasms
group Digestive System Diseases; Neoplasms Neoplastic Process 93 21 0.010 None 1.000 1 2006 2006
CUI: C0278592
Disease: Adult Angiosarcoma
Adult Angiosarcoma
disease Neoplasms Neoplastic Process 101 1 0.020 None 1.000 2 2018 2019
CUI: C0279988
Disease: Childhood Angiosarcoma
Childhood Angiosarcoma
disease Neoplasms Neoplastic Process 101 1 0.020 None 1.000 2 2018 2019
Leukocyte adhesion deficiency type 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases Disease or Syndrome 114 26 0.010 None 1.000 1 2016 2016
CUI: C4721698
Disease: Metastatic Renal Cell Carcinoma
Metastatic Renal Cell Carcinoma
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Neoplastic Process 144 9 0.010 None 1.000 1 2009 2009
CUI: C0278678
Disease: Metastatic Renal Cell Cancer
Metastatic Renal Cell Cancer
disease Neoplastic Process 145 9 0.010 None 1.000 1 2009 2009
CUI: C0544886
Disease: Somatic mutation
Somatic mutation
phenotype Cell or Molecular Dysfunction 151 0.100 None 0
CUI: C0238339
Disease: Hereditary pancreatitis
Hereditary pancreatitis
disease Digestive System Diseases Disease or Syndrome 158 108 0.010 None 1.000 1 2007 2007
CUI: C0023462
Disease: Acute Megakaryocytic Leukemias
Acute Megakaryocytic Leukemias
disease Neoplasms Neoplastic Process 159 15 0.010 None 1.000 1 2012 2012
CUI: C0018923
Disease: Hemangiosarcoma
Hemangiosarcoma
disease Neoplasms Neoplastic Process 162 7 0.020 None 1.000 2 2018 2019
CUI: C1527349
Disease: Ductal Breast Carcinoma
Ductal Breast Carcinoma
disease Neoplasms Neoplastic Process 196 10 0.010 None 1.000 1 2006 2006
CUI: C0333983
Disease: Hyperplastic Polyp
Hyperplastic Polyp
disease Pathological Conditions, Signs and Symptoms Neoplastic Process 204 22 0.010 None 1.000 1 2007 2007
CUI: C0040420
Disease: Tonometry
Tonometry
phenotype Diagnostic Procedure 206 573 0.100 None 1.000 2 2 2018 2018