CLDN10, claudin 10, 9071

N. diseases: 62; N. variants: 7
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4522164
Disease: HELIX SYNDROME
HELIX SYNDROME 		0.610 CausalMutation disease CLINVAR
CUI: C0151714
Disease: Hypermagnesemia
Hypermagnesemia 		0.110 Biomarker disease HPO
CUI: C0020599
Disease: Hypocalciuria
Hypocalciuria 		0.100 Biomarker phenotype HPO
CUI: C0020620
Disease: Hypohidrosis
Hypohidrosis 		0.100 Biomarker disease HPO
CUI: C0020621
Disease: Hypokalemia
Hypokalemia 		0.100 Biomarker phenotype HPO
CUI: C0032617
Disease: Polyuria
Polyuria 		0.100 Biomarker phenotype HPO
CUI: C0043352
Disease: Xerostomia
Xerostomia 		0.100 Biomarker disease HPO
CUI: C0085602
Disease: Polydipsia
Polydipsia 		0.100 Biomarker phenotype HPO
CUI: C0151908
Disease: Dry skin
Dry skin 		0.100 Biomarker phenotype HPO
CUI: C0231274
Disease: Intolerant of heat
Intolerant of heat 		0.100 Biomarker phenotype HPO
CUI: C0344505
Disease: Alacrima
Alacrima 		0.100 Biomarker disease HPO
CUI: C1522135
Disease: Hypermagnesemia result
Hypermagnesemia result 		0.100 Biomarker phenotype HPO
CUI: C1565489
Disease: Renal Insufficiency
Renal Insufficiency 		0.100 Biomarker disease HPO
CUI: C1963094
Disease: Dry Skin, CTCAE
Dry Skin, CTCAE 		0.100 Biomarker phenotype HPO
CUI: C4554647
Disease: Hypermagnesemia, CTCAE
Hypermagnesemia, CTCAE 		0.100 Biomarker phenotype HPO
CUI: C0012739
Disease: Disseminated Intravascular Coagulation
Disseminated Intravascular Coagulation 		0.010 Biomarker disease BEFREE <b>Abbreviations:</b> DAMA, discharged against medical advice; DIC, disseminated intravascular coagulation; HELIX, Hypothermia for Encephalopathy in Low- and Middle-Income Countries Trial; HIE, hypoxic ischaemic encephalopathy; IP, ice packs; LMIC, low- and middle-income countries; NICHD, National Institute of Child Health and Human Development; PCM, phase changing; TH, therapeutic hypothermia (TH); TOBY, total body hypothermia for neonatal encephalopathy. 30109814 2019
CUI: C0085584
Disease: Encephalopathies
Encephalopathies 		0.020 GeneticVariation group BEFREE <b>Abbreviations:</b> DAMA, discharged against medical advice; DIC, disseminated intravascular coagulation; HELIX, Hypothermia for Encephalopathy in Low- and Middle-Income Countries Trial; HIE, hypoxic ischaemic encephalopathy; IP, ice packs; LMIC, low- and middle-income countries; NICHD, National Institute of Child Health and Human Development; PCM, phase changing; TH, therapeutic hypothermia (TH); TOBY, total body hypothermia for neonatal encephalopathy. 30109814 2019
CUI: C0752304
Disease: Hypoxic-Ischemic Encephalopathy
Hypoxic-Ischemic Encephalopathy 		0.010 Biomarker disease BEFREE <b>Abbreviations:</b> DAMA, discharged against medical advice; DIC, disseminated intravascular coagulation; HELIX, Hypothermia for Encephalopathy in Low- and Middle-Income Countries Trial; HIE, hypoxic ischaemic encephalopathy; IP, ice packs; LMIC, low- and middle-income countries; NICHD, National Institute of Child Health and Human Development; PCM, phase changing; TH, therapeutic hypothermia (TH); TOBY, total body hypothermia for neonatal encephalopathy. 30109814 2019
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		0.030 Biomarker phenotype BEFREE <i>In vitro</i>, CLDN10 could promote cellular proliferation, migration, and invasion in PTC cell lines. 30588256 2018
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.010 GeneticVariation disease BEFREE 65 YEARS OF THE DOUBLE HELIX: One gene, many endocrine and metabolic syndromes: <i>PTEN</i>-opathies and precision medicine. 29792313 2018
CUI: C0031511
Disease: Pheochromocytoma
Pheochromocytoma 		0.010 Biomarker disease BEFREE 65 YEARS OF THE DOUBLE HELIX: Genetics informs precision practice in the diagnosis and management of pheochromocytoma. 29794110 2018
CUI: C4551683
Disease: Adrenal Gland Pheochromocytoma
Adrenal Gland Pheochromocytoma 		0.010 Biomarker disease BEFREE 65 YEARS OF THE DOUBLE HELIX: Genetics informs precision practice in the diagnosis and management of pheochromocytoma. 29794110 2018
CUI: C1333600
Disease: Hereditary Malignant Neoplasm
Hereditary Malignant Neoplasm 		0.010 GeneticVariation disease BEFREE 65 YEARS OF THE DOUBLE HELIX: The advancements of gene editing and potential application to hereditary cancer. 29980644 2018
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 Biomarker group BEFREE 65 YEARS OF THE DOUBLE HELIX: Classification of endocrine tumors in the age of integrated genomics. 29980645 2018
CUI: C1961099
Disease: Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma 		0.010 Biomarker disease BEFREE T-cell acute lymphoblastic leukemia and the associated basic helix-loop-helix gene SCL/tal. 8167548 1994