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: 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: C0478099
Disease: Other deletions of part of a chromosome
Other deletions of part of a chromosome 		disease 0.200 None 1.000 3 0 2004 2011
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C4303547
Disease: BNAR syndrome
BNAR syndrome 		disease 0.030 None 0.667 3 0 2011 2013
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: C0795830
Disease: CHROMOSOME 9p DELETION SYNDROME
CHROMOSOME 9p DELETION SYNDROME 		disease 0.200 None 1.000 3 0 2004 2011
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: C0265425
Disease: 9p partial monosomy syndrome
9p partial monosomy syndrome 		disease 0.200 None 1.000 3 0 2004 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: 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: 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: 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: 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: C0242473
Disease: Anus Prolapse
Anus Prolapse 		disease 0.010 None 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: C1619700
Disease: RENAL ADYSPLASIA
RENAL ADYSPLASIA 		disease 0.010 None 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: 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: 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: C1968949
Disease: Cakut
Cakut 		disease 0.010 None 1.000 1 0 2014 2014
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C0542519
Disease: Congenital absence of kidney
Congenital absence of kidney 		disease 0.010 None 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: C2363741
Disease: HIV-1 infection
HIV-1 infection 		disease 0.010 None 1.000 1 0 2012 2012
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C0001815
Disease: Primary Myelofibrosis
Primary Myelofibrosis 		disease 0.010 None 1.000 1 0 2019 2019
Entrez Id: 158326
Gene Symbol: FREM1
FREM1 		FRAS1 related extracellular matrix 1 0.633 0.423 1.6E-52
CUI: C0432122
Disease: Interfrontal craniofaciosynostosis
Interfrontal craniofaciosynostosis 		disease 0.010 None 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: C0003119
Disease: Anophthalmos
Anophthalmos 		disease 0.100 None 0 0