WNT5A, Wnt family member 5A, 7474

N. diseases: 375; N. variants: 11
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: C0231450
Disease: Abnormal extension
Abnormal extension 		phenotype Sign or Symptom 1 0.010 None 1.000 1 2017 2017
CUI: C1719710
Disease: Chronic post-thoracotomy pain
Chronic post-thoracotomy pain 		phenotype Pathological Conditions, Signs and Symptoms Disease or Syndrome 2 0.020 None 1.000 2 2017 2018
CUI: C4551475
Disease: ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 3 11 0.600 strong 1.000 1 6 2010 2010
CUI: C4551476
Disease: Robinow Syndrome, Autosomal Dominant
Robinow Syndrome, Autosomal Dominant 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 4 0.330 None 1.000 3 2010 2015
CUI: C1849343
Disease: Duplication of the distal phalanx of hand
Duplication of the distal phalanx of hand 		phenotype Finding 4 0.100 None 0
CUI: C4021772
Disease: Bifid distal phalanx of toe
Bifid distal phalanx of toe 		disease Anatomical Abnormality 4 0.100 None 0
CUI: C4022477
Disease: Onychogryposis of fingernail
Onychogryposis of fingernail 		phenotype Finding 4 0.100 None 0
CUI: C0266304
Disease: Double kidney (disorder)
Double kidney (disorder) 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 6 0.010 None 1.000 1 2017 2017
CUI: C3827253
Disease: Classical Glioblastoma
Classical Glioblastoma 		disease Neoplastic Process 6 2 0.010 None 1.000 1 2017 2017
CUI: C1854409
Disease: Naevus flammeus of the eyelid
Naevus flammeus of the eyelid 		phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Finding 6 0.100 None 0
CUI: C4023918
Disease: Short hard palate
Short hard palate 		disease Anatomical Abnormality 7 4 0.100 None 0
CUI: C0796013
Disease: Zimmerman Laband syndrome
Zimmerman Laband syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases Disease or Syndrome 8 0.020 None 1.000 2 2007 2007
CUI: C1303001
Disease: Congenital euryblepharon
Congenital euryblepharon 		disease Congenital Abnormality 9 0.100 None 0
CUI: C1849392
Disease: Ridged fingernail
Ridged fingernail 		phenotype Finding 9 0.100 None 0
CUI: C1865038
Disease: Broad toe
Broad toe 		phenotype Finding 11 2 0.100 None 0
CUI: C4020952
Disease: Fingernail dysplasia
Fingernail dysplasia 		disease Disease or Syndrome 11 0.100 None 0
CUI: C1849341
Disease: Triangular mouth
Triangular mouth 		phenotype Finding 14 0.100 None 0
CUI: C0220624
Disease: Adult Brain Neoplasm
Adult Brain Neoplasm 		disease Neoplasms; Nervous System Diseases Neoplastic Process 15 0.010 None 1.000 1 2007 2007
CUI: C3554224
Disease: LEPTIN DEFICIENCY OR DYSFUNCTION
LEPTIN DEFICIENCY OR DYSFUNCTION 		disease Disease or Syndrome 15 3 0.010 None 1.000 1 2014 2014
CUI: C2673670
Disease: Curly eyelashes
Curly eyelashes 		phenotype Finding 15 0.100 None 0
CUI: C2750604
Disease: Median cleft lip and palate
Median cleft lip and palate 		disease Congenital Abnormality 15 0.100 None 0
CUI: C0264511
Disease: Lymphoid interstitial pneumonia
Lymphoid interstitial pneumonia 		disease Respiratory Tract Diseases Disease or Syndrome 17 0.010 None 1.000 1 2020 2020
CUI: C1834060
Disease: Short middle phalanx of the 5th finger
Short middle phalanx of the 5th finger 		phenotype Finding 17 0.100 None 0
CUI: C1720887
Disease: Female Urogenital Diseases
Female Urogenital Diseases 		group Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 18 0.300 None 1.000 1 2005 2005
CUI: C0019288
Disease: Hernia, Femoral
Hernia, Femoral 		disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 18 0.100 None 0