PC Results

MLH1

mutL homolog 1
08/22/2019

MSH2

mutS homolog 2
08/22/2019

PMS2

PMS1 homolog 2, mismatch repair system component
08/22/2019

PCSK9

proprotein convertase subtilisin/kexin type 9
11/14/2018

MYBPC3

myosin binding protein C, cardiac
08/22/2019

SMAD4

SMAD family member 4
08/22/2019

EPCAM

epithelial cell adhesion molecule
10/08/2019

PKD2

polycystin 2, transient receptor potential cation channel
08/22/2019

APC

APC, WNT signaling pathway regulator
08/22/2019

PCDH15

protocadherin related 15
10/22/2018

GCH1

GTP cyclohydrolase 1
08/22/2019

GPC3

glypican 3
12/31/2019

FOXP1

forkhead box P1
01/22/2020

KCNQ2

potassium voltage-gated channel subfamily Q member 2
08/22/2019

SLC16A2

solute carrier family 16 member 2
08/22/2019

PCCA

propionyl-CoA carboxylase subunit alpha
12/13/2018

GIPC3

GIPC PDZ domain containing family member 3
10/22/2018

PCDH19

protocadherin 19
08/22/2019

MALT1

MALT1 paracaspase
10/22/2018

ADAMTS2

ADAM metallopeptidase with thrombospondin type 1 motif 2
11/12/2018

APC-related attenuated familial adenomatous polyposis

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

sessile serrated polyposis cancer syndrome; SSPCS

MONDO_0014919 Condition
Sessile Serrated Polyposis Cancer Syndrome
10/23/2017

PCWH syndrome

MONDO_0012198 Condition
WS4 plus

HPCX2

MONDO_0010405 Condition

HPC14

MONDO_0012769 Condition

MCOPCB2

MONDO_0011589 Condition

HPC15

MONDO_0012770 Condition

PCD

MONDO_0008932 Condition

MCOPCB1

MONDO_0024549 Condition

HPCX1

MONDO_0010257 Condition

MCOPCT1

MONDO_0007995 Condition

polycystic liver disease 2; PCLD2

MONDO_0014860 Condition
PCLD2

palmoplantar carcinoma, multiple self-healing; MSPC

MONDO_0014852 Condition
Palmoplantar Carcinoma, Multiple Self-Healing

HPC11

MONDO_0012768 Condition

PCNA-related progressive neurodegenerative photosensitivy syndrome

MONDO_0014399 Condition
Ataxia-Telangiectasia-Like Disorder type 2

pontocerebellar hypoplasia, type 2F; PCH2F

MONDO_0014874 Condition
PCH2F

autosomal recessive severe congenital neutropenia due to G6PC3 deficiency

MONDO_0012930 Condition
Severe congenital neutropenia-pulmonary hypertension-superficial venous angiectasis syndrome

HPC7

MONDO_0012470 Condition

HPC10

MONDO_0012620 Condition