CDC42, cell division cycle 42, 998

N. diseases: 327; 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: C4225222
Disease: TAKENOUCHI-KOSAKI SYNDROME
TAKENOUCHI-KOSAKI SYNDROME 		disease Disease or Syndrome 1 6 0.710 None 1.000 4 6 2015 2018
CUI: C0741146
Disease: anxiety acute
anxiety acute 		disease Mental or Behavioral Dysfunction 1 0.010 None 1.000 1 2014 2014
CUI: C0596848
Disease: lipoprotein disorder
lipoprotein disorder 		disease Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 3 0.010 None 1.000 1 2000 2000
CUI: C1845987
Disease: Neutropenia, Severe Congenital, X-Linked
Neutropenia, Severe Congenital, X-Linked 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 4 14 0.010 None < 0.001 1 2013 2013
CUI: C0277873
Disease: Nasal Flaring
Nasal Flaring 		phenotype Sign or Symptom 5 0.100 None 0
CUI: C1835801
Disease: Eversion of lateral third of lower eyelids
Eversion of lateral third of lower eyelids 		phenotype Eye Diseases Finding 6 0.100 None 0
CUI: C4551517
Disease: Flared nostrils abnormality
Flared nostrils abnormality 		phenotype Finding 6 1 0.100 None 0
CUI: C1337012
Disease: Well-differentiated papillary mesothelioma
Well-differentiated papillary mesothelioma 		disease Neoplasms Neoplastic Process 9 0.010 None 1.000 1 2019 2019
CUI: C1096367
Disease: Increased mean platelet volume
Increased mean platelet volume 		phenotype Finding 10 2 0.100 None 0
CUI: C1519787
Disease: Undifferentiated Neuroblastoma
Undifferentiated Neuroblastoma 		disease Neoplasms Neoplastic Process 12 0.010 None 1.000 1 2014 2014
CUI: C4021866
Disease: obsolete Abnormal heart morphology
obsolete Abnormal heart morphology 		phenotype Anatomical Abnormality 12 13 0.100 None 0 1
CUI: C0334246
Disease: Squamous cell carcinoma, metastatic
Squamous cell carcinoma, metastatic 		disease Neoplasms Neoplastic Process 13 0.010 None 1.000 1 2011 2011
CUI: C1412000
Disease: Mesenteric vascular insufficiency
Mesenteric vascular insufficiency 		disease Digestive System Diseases; Cardiovascular Diseases Disease or Syndrome 13 0.010 None 1.000 1 2017 2017
CUI: C4551482
Disease: Adams-Oliver syndrome 1
Adams-Oliver syndrome 1 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 17 9 0.010 None 1.000 1 2011 2011
CUI: C4289709
Disease: DOCK8 Deficiency
DOCK8 Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 18 0.010 None 1.000 1 2017 2017
CUI: C0341306
Disease: Microvillus inclusion disease
Microvillus inclusion disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 19 16 0.010 None 1.000 1 2016 2016
CUI: C0750887
Disease: Adrenal Cancer
Adrenal Cancer 		disease Neoplasms; Endocrine System Diseases Neoplastic Process 20 0.300 None 1.000 1 2014 2014
CUI: C0028866
Disease: Oculomotor Nerve Paralysis
Oculomotor Nerve Paralysis 		disease Eye Diseases; Nervous System Diseases Disease or Syndrome 22 1 0.100 None 0 1
CUI: C0272139
Disease: Erythrocytosis due to low atmospheric pressure
Erythrocytosis due to low atmospheric pressure 		disease Hemic and Lymphatic Diseases Disease or Syndrome 25 13 0.010 None 1.000 1 2012 2012
CUI: C0282606
Disease: Myomatous neoplasm
Myomatous neoplasm 		disease Neoplasms; Musculoskeletal Diseases Neoplastic Process 25 0.010 None 1.000 1 2002 2002
CUI: C3539920
Disease: ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE
ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE 		disease Disease or Syndrome 25 7 0.010 None 1.000 1 2005 2005
CUI: C3887494
Disease: ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE
ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 25 35 0.010 None 1.000 1 2005 2005
CUI: C0043046
Disease: Wasting Syndrome
Wasting Syndrome 		disease Nutritional and Metabolic Diseases Disease or Syndrome 26 2 0.010 None 1.000 1 2018 2018
CUI: C0600452
Disease: Hepatopulmonary Syndrome
Hepatopulmonary Syndrome 		disease Digestive System Diseases; Respiratory Tract Diseases Disease or Syndrome 29 1 0.010 None 1.000 1 2019 2019
CUI: C3809250
Disease: ESTROGEN RESISTANCE
ESTROGEN RESISTANCE 		disease Disease or Syndrome 30 7 0.010 None 1.000 1 2007 2007