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: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C1855425
Disease: Marles Greenberg Persaud syndrome
Marles Greenberg Persaud syndrome 		disease 0.750 None 0.875 8 3 2001 2017
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C2750433
Disease: Bifid Nose With Or Without Anorectal And Renal Anomalies
Bifid Nose With Or Without Anorectal And Renal Anomalies 		disease 0.720 None 0.800 5 2 2001 2014
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C0265535
Disease: Trigonocephaly
Trigonocephaly 		disease 0.700 limited 1.000 1 0 2011 2011
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C0221363
Disease: Bifid nose
Bifid nose 		disease 0.620 limited 1.000 3 0 2011 2013
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C3280974
Disease: TRIGONOCEPHALY 2
TRIGONOCEPHALY 2 		disease 0.600 limited 1.000 2 2 2001 2011
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C1609433
Disease: Congenital absence of kidneys syndrome
Congenital absence of kidneys syndrome 		disease 0.410 None 1.000 2 0 2011 2013
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C1860819
Disease: Metopic synostosis
Metopic synostosis 		disease 0.400 None 0 0
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C0235833
Disease: Congenital diaphragmatic hernia
Congenital diaphragmatic hernia 		disease 0.320 None 1.000 3 0 2013 2018
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C0265699
Disease: Congenital hernia of foramen of Morgagni
Congenital hernia of foramen of Morgagni 		disease 0.300 None 1.000 2 0 2013 2016
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C0265700
Disease: Congenital hernia of foramen of Bochdalek
Congenital hernia of foramen of Bochdalek 		disease 0.300 None 1.000 2 0 2013 2016
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C0266294
Disease: Unilateral agenesis of kidney
Unilateral agenesis of kidney 		disease 0.300 None 1.000 2 0 2010 2014
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C0015393
Disease: Eye Abnormalities
Eye Abnormalities 		group 0.300 None 1.000 1 0 2013 2013
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C2751431
Disease: Bifid Nose, Autosomal Dominant
Bifid Nose, Autosomal Dominant 		disease 0.300 None 1.000 1 0 2013 2013
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C3887497
Disease: Bifid Nose, Autosomal Recessive
Bifid Nose, Autosomal Recessive 		disease 0.300 None 1.000 1 0 2013 2013
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C0265534
Disease: Scaphycephaly
Scaphycephaly 		disease 0.300 None 0 0
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C1833340
Disease: Synostotic Posterior Plagiocephaly
Synostotic Posterior Plagiocephaly 		disease 0.300 None 0 0
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C4551902
Disease: Craniosynostosis, Type 1
Craniosynostosis, Type 1 		disease 0.300 None 0 0
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C2931150
Disease: Synostotic Anterior Plagiocephaly
Synostotic Anterior Plagiocephaly 		disease 0.300 None 0 0
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis 		disease 0.300 None 0 0
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C0015397
Disease: Disorder of eye
Disorder of eye 		group 0.300 limited 0 0
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C0030044
Disease: Acrocephaly
Acrocephaly 		disease 0.300 None 0 0
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C0221356
Disease: Brachycephaly
Brachycephaly 		disease 0.300 None 0 0
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C0265233
Disease: Cryptophthalmos syndrome
Cryptophthalmos syndrome 		disease 0.240 None 1.000 4 0 2011 2018
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C0019284
Disease: Diaphragmatic Hernia
Diaphragmatic Hernia 		phenotype 0.210 None 1.000 3 0 2013 2016
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C0265425
Disease: 9p partial monosomy syndrome
9p partial monosomy syndrome 		disease 0.200 None 1.000 3 0 2004 2011