Source: INFERRED

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
WD repeat domain 35 0.525 0.692 1.0E-22
SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY
disease 0.920 None 1.000 8 13 2007 2018
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
WD repeat domain 35 0.525 0.692 1.0E-22
CUI: C3150874
Disease: CRANIOECTODERMAL DYSPLASIA 2
CRANIOECTODERMAL DYSPLASIA 2
disease 0.600 None 1.000 7 16 2010 2018
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
WD repeat domain 35 0.525 0.692 1.0E-22
SHORT-RIB THORACIC DYSPLASIA 7/20 WITH POLYDACTYLY, DIGENIC
disease 0.600 None 1.000 0 1 2007 2011
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
WD repeat domain 35 0.525 0.692 1.0E-22
CUI: C0036996
Disease: Short Rib-Polydactyly Syndrome
Short Rib-Polydactyly Syndrome
disease 0.420 None 1.000 0 4 2011 2019
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
WD repeat domain 35 0.525 0.692 1.0E-22
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis
disease 0.410 None 1.000 0 0 2010 2013
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
WD repeat domain 35 0.525 0.692 1.0E-22
CUI: C1860819
Disease: Metopic synostosis
Metopic synostosis
disease 0.400 None 1.000 0 0 2010 2010
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
WD repeat domain 35 0.525 0.692 1.0E-22
CUI: C4551571
Disease: Cranioectodermal dysplasia
Cranioectodermal dysplasia
disease 0.190 None 1.000 3 8 2010 2019
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
WD repeat domain 35 0.525 0.692 1.0E-22
CUI: C0152427
Disease: Polydactyly
Polydactyly
disease 0.120 None 1.000 0 0 2011 2012
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
WD repeat domain 35 0.525 0.692 1.0E-22
CUI: C4021790
Disease: Abnormality of the skeletal system
Abnormality of the skeletal system
disease 0.110 None 1.000 0 1 2018 2018
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
WD repeat domain 35 0.525 0.692 1.0E-22
CUI: C0265275
Disease: Jeune thoracic dystrophy
Jeune thoracic dystrophy
disease 0.110 None 1.000 0 4 2019 2019
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
WD repeat domain 35 0.525 0.692 1.0E-22
CUI: C0266449
Disease: Congenital anomaly of brain
Congenital anomaly of brain
group 0.110 None 1.000 0 1 2018 2018
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
WD repeat domain 35 0.525 0.692 1.0E-22
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
phenotype 0.100 None 1.000 1 1 2012 2012
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
WD repeat domain 35 0.525 0.692 1.0E-22
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
WD repeat domain 35 0.525 0.692 1.0E-22
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
WD repeat domain 35 0.525 0.692 1.0E-22
CUI: C1837770
Disease: Sparse hair
Sparse hair
phenotype 0.100 None 0 0
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
WD repeat domain 35 0.525 0.692 1.0E-22
CUI: C1837485
Disease: Flat acetabular roof
Flat acetabular roof
phenotype 0.100 None 0 0
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
WD repeat domain 35 0.525 0.692 1.0E-22
CUI: C1839829
Disease: Short distal phalanx of finger
Short distal phalanx of finger
phenotype 0.100 None 0 0
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
WD repeat domain 35 0.525 0.692 1.0E-22
CUI: C1836542
Disease: Depressed nasal bridge
Depressed nasal bridge
phenotype 0.100 None 0 0
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
WD repeat domain 35 0.525 0.692 1.0E-22
CUI: C1848701
Disease: Elevated hepatic transaminase
Elevated hepatic transaminase
phenotype 0.100 None 0 0
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
WD repeat domain 35 0.525 0.692 1.0E-22
CUI: C1839758
Disease: Narrow forehead
Narrow forehead
phenotype 0.100 None 0 0
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
WD repeat domain 35 0.525 0.692 1.0E-22
CUI: C1840077
Disease: Anteverted nostril
Anteverted nostril
phenotype 0.100 None 0 0
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
WD repeat domain 35 0.525 0.692 1.0E-22
CUI: C1843108
Disease: Short palm
Short palm
phenotype 0.100 None 0 0
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
WD repeat domain 35 0.525 0.692 1.0E-22
CUI: C1843300
Disease: Sparse eyelashes
Sparse eyelashes
phenotype 0.100 None 0 0
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
WD repeat domain 35 0.525 0.692 1.0E-22
CUI: C1844813
Disease: Widely spaced teeth
Widely spaced teeth
phenotype 0.100 None 0 0
Entrez Id: 57539
Gene Symbol: WDR35
WDR35
WD repeat domain 35 0.525 0.692 1.0E-22
CUI: C1846434
Disease: Hypoplastic scapulae
Hypoplastic scapulae
phenotype 0.100 None 0 0