Source: ALL

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: 55764
Gene Symbol: IFT122
IFT122 		intraflagellar transport 122 0.560 0.846 2.4E-24
CUI: C0432235
Disease: CRANIOECTODERMAL DYSPLASIA 1
CRANIOECTODERMAL DYSPLASIA 1 		disease 0.730 None 1.000 10 10 2009 2018
Entrez Id: 55764
Gene Symbol: IFT122
IFT122 		intraflagellar transport 122 0.560 0.846 2.4E-24
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis 		disease 0.400 None 1.000 1 0 2010 2010
Entrez Id: 55764
Gene Symbol: IFT122
IFT122 		intraflagellar transport 122 0.560 0.846 2.4E-24
CUI: C0265534
Disease: Scaphycephaly
Scaphycephaly 		disease 0.400 None 1.000 1 0 2010 2010
Entrez Id: 55764
Gene Symbol: IFT122
IFT122 		intraflagellar transport 122 0.560 0.846 2.4E-24
CUI: C0011989
Disease: Camurati-Engelmann Syndrome
Camurati-Engelmann Syndrome 		disease 0.320 strong 1.000 3 0 2000 2018
Entrez Id: 55764
Gene Symbol: IFT122
IFT122 		intraflagellar transport 122 0.560 0.846 2.4E-24
CUI: C0432198
Disease: Short rib-polydactyly syndrome, Beemer type
Short rib-polydactyly syndrome, Beemer type 		disease 0.310 None 1.000 1 0 2017 2017
Entrez Id: 55764
Gene Symbol: IFT122
IFT122 		intraflagellar transport 122 0.560 0.846 2.4E-24
CUI: C2931150
Disease: Synostotic Anterior Plagiocephaly
Synostotic Anterior Plagiocephaly 		disease 0.300 None 1.000 1 0 2010 2010
Entrez Id: 55764
Gene Symbol: IFT122
IFT122 		intraflagellar transport 122 0.560 0.846 2.4E-24
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases 		group 0.300 None 1.000 1 0 2010 2010
Entrez Id: 55764
Gene Symbol: IFT122
IFT122 		intraflagellar transport 122 0.560 0.846 2.4E-24
CUI: C0549423
Disease: Obstructive Hydrocephalus
Obstructive Hydrocephalus 		disease 0.300 None 1.000 1 0 2010 2010
Entrez Id: 55764
Gene Symbol: IFT122
IFT122 		intraflagellar transport 122 0.560 0.846 2.4E-24
CUI: C0265535
Disease: Trigonocephaly
Trigonocephaly 		disease 0.300 None 1.000 1 0 2010 2010
Entrez Id: 55764
Gene Symbol: IFT122
IFT122 		intraflagellar transport 122 0.560 0.846 2.4E-24
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus 		disease 0.300 None 1.000 1 0 2010 2010
Entrez Id: 55764
Gene Symbol: IFT122
IFT122 		intraflagellar transport 122 0.560 0.846 2.4E-24
CUI: C1860819
Disease: Metopic synostosis
Metopic synostosis 		disease 0.300 None 1.000 1 0 2010 2010
Entrez Id: 55764
Gene Symbol: IFT122
IFT122 		intraflagellar transport 122 0.560 0.846 2.4E-24
CUI: C1531647
Disease: Cerebral ventriculomegaly
Cerebral ventriculomegaly 		phenotype 0.300 None 1.000 1 0 2010 2010
Entrez Id: 55764
Gene Symbol: IFT122
IFT122 		intraflagellar transport 122 0.560 0.846 2.4E-24
CUI: C0030044
Disease: Acrocephaly
Acrocephaly 		disease 0.300 None 1.000 1 0 2010 2010
Entrez Id: 55764
Gene Symbol: IFT122
IFT122 		intraflagellar transport 122 0.560 0.846 2.4E-24
CUI: C0270720
Disease: Hydrocephalus Ex-Vacuo
Hydrocephalus Ex-Vacuo 		disease 0.300 None 1.000 1 0 2010 2010
Entrez Id: 55764
Gene Symbol: IFT122
IFT122 		intraflagellar transport 122 0.560 0.846 2.4E-24
CUI: C2936786
Disease: Aqueductal Stenosis
Aqueductal Stenosis 		disease 0.300 None 1.000 1 0 2010 2010
Entrez Id: 55764
Gene Symbol: IFT122
IFT122 		intraflagellar transport 122 0.560 0.846 2.4E-24
CUI: C0037932
Disease: Curvature of spine
Curvature of spine 		phenotype 0.300 None 1.000 1 0 2010 2010
Entrez Id: 55764
Gene Symbol: IFT122
IFT122 		intraflagellar transport 122 0.560 0.846 2.4E-24
CUI: C0221356
Disease: Brachycephaly
Brachycephaly 		disease 0.300 None 1.000 1 0 2010 2010
Entrez Id: 55764
Gene Symbol: IFT122
IFT122 		intraflagellar transport 122 0.560 0.846 2.4E-24
CUI: C1833340
Disease: Synostotic Posterior Plagiocephaly
Synostotic Posterior Plagiocephaly 		disease 0.300 None 1.000 1 0 2010 2010
Entrez Id: 55764
Gene Symbol: IFT122
IFT122 		intraflagellar transport 122 0.560 0.846 2.4E-24
CUI: C2936718
Disease: Fetal Cerebral Ventriculomegaly
Fetal Cerebral Ventriculomegaly 		disease 0.300 None 1.000 1 0 2010 2010
Entrez Id: 55764
Gene Symbol: IFT122
IFT122 		intraflagellar transport 122 0.560 0.846 2.4E-24
CUI: C0009451
Disease: Communicating Hydrocephalus
Communicating Hydrocephalus 		disease 0.300 None 1.000 1 0 2010 2010
Entrez Id: 55764
Gene Symbol: IFT122
IFT122 		intraflagellar transport 122 0.560 0.846 2.4E-24
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		group 0.300 None 1.000 1 0 2010 2010
Entrez Id: 55764
Gene Symbol: IFT122
IFT122 		intraflagellar transport 122 0.560 0.846 2.4E-24
CUI: C0013608
Disease: Edema, Cardiac
Edema, Cardiac 		disease 0.300 None 1.000 1 0 2010 2010
Entrez Id: 55764
Gene Symbol: IFT122
IFT122 		intraflagellar transport 122 0.560 0.846 2.4E-24
CUI: C0015393
Disease: Eye Abnormalities
Eye Abnormalities 		group 0.300 None 1.000 1 0 2010 2010
Entrez Id: 55764
Gene Symbol: IFT122
IFT122 		intraflagellar transport 122 0.560 0.846 2.4E-24
CUI: C4551720
Disease: Primary Ciliary Dyskinesia
Primary Ciliary Dyskinesia 		disease 0.300 None 1.000 1 0 2010 2010
Entrez Id: 55764
Gene Symbol: IFT122
IFT122 		intraflagellar transport 122 0.560 0.846 2.4E-24
CUI: C4551902
Disease: Craniosynostosis, Type 1
Craniosynostosis, Type 1 		disease 0.300 None 1.000 1 0 2010 2010