Rel Results

CRTAP

cartilage associated protein
10/17/2018

10/10/2018

SLC35D1

solute carrier family 35 member D1
05/31/2017

AREL1

apoptosis resistant E3 ubiquitin protein ligase 1

CRELD1

cysteine rich with EGF like domains 1

CRELD2

cysteine rich with EGF like domains 2

GGT5

gamma-glutamyltransferase 5

IL17REL

interleukin 17 receptor E like

KIRREL1

kirre like nephrin family adhesion molecule 1

KIRREL2

kirre like nephrin family adhesion molecule 2

KIRREL3

kirre like nephrin family adhesion molecule 3

PRELID1

PRELI domain containing 1

PRELID2

PRELI domain containing 2

PRELID3A

PRELI domain containing 3A

PRELID3B

PRELI domain containing 3B

PRELP

proline and arginine rich end leucine rich repeat protein

REG4

regenerating family member 4

REL

REL proto-oncogene, NF-kB subunit

RELA

RELA proto-oncogene, NF-kB subunit

RELB

RELB proto-oncogene, NF-kB subunit

MUTYH-related attenuated familial adenomatous polyposis

MONDO_0012041 Condition
MUTYH-related attenuated familial polyposis coli
05/08/2018

12/11/2017

BAP1-related tumor predisposition syndrome

MONDO_0013692 Condition
Tumor susceptibility linked to germline BAP1 mutations
10/12/2018

APC-related attenuated familial adenomatous polyposis

MONDO_0016613 Condition
APC-related attenuated FAP
09/11/2017

04/27/2018

MSH3-related attenuated familial adenomatous polyposis

MONDO_0018812 Condition
MSH3-related attenuated FAP
12/13/2016

FADD-related immunodeficiency

MONDO_0013408 Condition
11/13/2018

PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation

MONDO_0014512 Condition
Mental Retardation, Autosomal Dominant type 31
02/07/2018

Birk-Barel syndrome

MONDO_0012856 Condition
Intellectual disability-hypotonia-facial dysmorphism syndrome
06/01/2017

NTHL1-related attenuated familial adenomatous polyposis

MONDO_0014630 Condition
Familial Adenomatous Polyposis type 3
06/08/2017

AXIN2-related attenuated familial adenomatous polyposis

MONDO_0018426 Condition
AXIN2-related AFAP
06/08/2017

MYH-9 related disease

MONDO_0015912 Condition
MYH9-related syndromic thrombocytopenia
07/17/2018

CIDEC-related familial partial lipodystrophy

MONDO_0014098 Condition
CIDEC-related FPLD
10/19/2018

age related macular degeneration 10

MONDO_0012674 Condition
age related macular degeneration type 10

asthma-related traits, susceptibility to, 6

MONDO_0012666 Condition
Asthma-Related Traits, Susceptibility To, type 6

asthma-related traits, susceptibility to, 4

MONDO_0012577 Condition
Asthma-Related Traits, Susceptibility To, type 4

age related macular degeneration 4

MONDO_0012540 Condition
age related macular degeneration type 4

phenol 14 MG/ML [Ora Relief]

RXNORM:643817 Drug