RHOA, ras homolog family member A, 387

N. diseases: 193; 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: C1744559
Disease: Congenital ectodermal dysplasia of face
Congenital ectodermal dysplasia of face 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 3 3 0.300 None 1.000 1 2019 2019
CUI: C0040435
Disease: Tooth Diseases
Tooth Diseases 		group Stomatognathic Diseases Disease or Syndrome 4 0.300 None 1.000 1 2019 2019
CUI: C0000771
Disease: Abnormalities, Drug-Induced
Abnormalities, Drug-Induced 		group Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 5 0.300 None 1.000 1 2015 2015
CUI: C0162361
Disease: Hidrotic Ectodermal Dysplasia
Hidrotic Ectodermal Dysplasia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 8 7 0.300 None 1.000 1 2019 2019
CUI: C0274306
Disease: Cutaneous anaphylaxis
Cutaneous anaphylaxis 		disease Immune System Diseases Disease or Syndrome 12 0.010 None 1.000 1 2015 2015
CUI: C0263477
Disease: Female pattern alopecia (disorder)
Female pattern alopecia (disorder) 		phenotype Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 15 0.300 None 1.000 1 2019 2019
CUI: C4531083
Disease: Mucinous gastric carcinoma
Mucinous gastric carcinoma 		disease Neoplastic Process 15 0.010 None 1.000 1 2016 2016
CUI: C0022876
Disease: Premature Obstetric Labor
Premature Obstetric Labor 		phenotype Female Urogenital Diseases and Pregnancy Complications Pathologic Function 18 0.010 None 1.000 1 2007 2007
CUI: C0265699
Disease: Congenital hernia of foramen of Morgagni
Congenital hernia of foramen of Morgagni 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 19 0.300 None 1.000 1 2015 2015
CUI: C2242635
Disease: Tumour thrombosis
Tumour thrombosis 		disease Neoplastic Process 19 0.010 None 1.000 1 2013 2013
CUI: C0342731
Disease: Deficiency of mevalonate kinase
Deficiency of mevalonate kinase 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases; Nervous System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 20 23 0.010 None 1.000 1 2014 2014
CUI: C0265700
Disease: Congenital hernia of foramen of Bochdalek
Congenital hernia of foramen of Bochdalek 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 21 0.300 None 1.000 1 2015 2015
CUI: C0376407
Disease: Granulomatous Slack Skin
Granulomatous Slack Skin 		disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 22 0.300 None 1.000 1 2015 2015
CUI: C1516061
Disease: Astler-Coller B1 Rectal Carcinoma
Astler-Coller B1 Rectal Carcinoma 		disease Neoplastic Process 22 1 0.010 None 1.000 1 2017 2017
CUI: C0086873
Disease: Pseudopelade
Pseudopelade 		disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 23 0.300 None 1.000 1 2019 2019
CUI: C0334279
Disease: Adenocarcinoma, intestinal type
Adenocarcinoma, intestinal type 		disease Neoplasms Neoplastic Process 23 2 0.010 None 1.000 1 2019 2019
CUI: C0265316
Disease: Neurocutaneous Syndromes
Neurocutaneous Syndromes 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Nervous System Diseases Disease or Syndrome 28 0.300 None 1.000 1 2019 2019
CUI: C1706004
Disease: Anhydrotic Ectodermal Dysplasias
Anhydrotic Ectodermal Dysplasias 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Congenital Abnormality 29 2 0.300 None 1.000 1 2019 2019
CUI: C0007192
Disease: Cardiomyopathy, Alcoholic
Cardiomyopathy, Alcoholic 		disease Chemically-Induced Disorders; Cardiovascular Diseases Disease or Syndrome 30 0.010 None 1.000 1 2019 2019
CUI: C0027814
Disease: Neuritis, Autoimmune, Experimental
Neuritis, Autoimmune, Experimental 		disease Immune System Diseases; Nervous System Diseases Experimental Model of Disease 32 0.200 None 1.000 1 2007 2007
CUI: C0343640
Disease: African Burkitt's lymphoma
African Burkitt's lymphoma 		disease Neoplasms; Infections; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 36 5 0.010 None < 0.001 1 2015 2015
CUI: C0014836
Disease: Escherichia coli Infections
Escherichia coli Infections 		group Infections Disease or Syndrome 38 0.010 None 1.000 1 2019 2019
CUI: C0264886
Disease: Conduction disorder of the heart
Conduction disorder of the heart 		group Cardiovascular Diseases Disease or Syndrome 41 11 0.010 None 1.000 1 2019 2019
CUI: C3828416
Disease: Radiation Damage
Radiation Damage 		disease Wounds and Injuries Disease or Syndrome 44 0.010 None 1.000 1 2017 2017
CUI: C1876214
Disease: ALBINOIDISM, OCULOCUTANEOUS, AUTOSOMAL DOMINANT
ALBINOIDISM, OCULOCUTANEOUS, AUTOSOMAL DOMINANT 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 54 6 0.010 None 1.000 1 2019 2019