CLDN10, claudin 10, 9071

N. diseases: 62; N. variants: 7
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C4522164
Disease: HELIX SYNDROME
HELIX SYNDROME 		disease Disease or Syndrome 1 3 0.610 moderate 1.000 3 3 2009 2018
CUI: C4520903
Disease: Stage 0 Lung Adenocarcinoma AJCC v6 and v7
Stage 0 Lung Adenocarcinoma AJCC v6 and v7 		disease Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 2 0.010 None 1.000 1 2013 2013
CUI: C4521520
Disease: Lung Adenocarcinoma In Situ
Lung Adenocarcinoma In Situ 		disease Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 2 0.010 None 1.000 1 2013 2013
CUI: C1522135
Disease: Hypermagnesemia result
Hypermagnesemia result 		phenotype Finding 7 1 0.100 None 0
CUI: C4554647
Disease: Hypermagnesemia, CTCAE
Hypermagnesemia, CTCAE 		phenotype Finding 7 0.100 None 0
CUI: C0151714
Disease: Hypermagnesemia
Hypermagnesemia 		disease Nutritional and Metabolic Diseases Disease or Syndrome 10 0.110 None 1.000 1 2018 2018
CUI: C0373607
Disease: Ferritin measurement
Ferritin measurement 		phenotype Laboratory Procedure 10 21 0.100 None 1.000 1 1 2017 2017
CUI: C0696113
Disease: Serum ferritin measurement
Serum ferritin measurement 		phenotype Laboratory Procedure 10 21 0.100 None 1.000 1 1 2017 2017
CUI: C0020599
Disease: Hypocalciuria
Hypocalciuria 		phenotype Nutritional and Metabolic Diseases Disease or Syndrome 16 4 0.100 None 0
CUI: C0344505
Disease: Alacrima
Alacrima 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 16 1 0.100 None 0
CUI: C0231274
Disease: Intolerant of heat
Intolerant of heat 		phenotype Pathologic Function 19 7 0.100 None 0
CUI: C0020256
Disease: Congenital Hydrocephalus
Congenital Hydrocephalus 		disease Nervous System Diseases Congenital Abnormality 39 0.010 None 1.000 1 1998 1998
CUI: C4049711
Disease: Lepidic Predominant Adenocarcinoma
Lepidic Predominant Adenocarcinoma 		disease Neoplasms Neoplastic Process 46 0.010 None 1.000 1 2013 2013
CUI: C0043352
Disease: Xerostomia
Xerostomia 		disease Stomatognathic Diseases Finding 56 1 0.100 None 0
CUI: C0151723
Disease: Hypomagnesemia
Hypomagnesemia 		phenotype Nutritional and Metabolic Diseases Disease or Syndrome 58 11 0.010 None 1.000 1 2018 2018
CUI: C0020621
Disease: Hypokalemia
Hypokalemia 		phenotype Nutritional and Metabolic Diseases Finding 61 7 0.100 None 0
CUI: C0085602
Disease: Polydipsia
Polydipsia 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 61 5 0.100 None 0
CUI: C1333600
Disease: Hereditary Malignant Neoplasm
Hereditary Malignant Neoplasm 		disease Neoplasms Neoplastic Process 63 18 0.010 None 1.000 1 2018 2018
CUI: C0020620
Disease: Hypohidrosis
Hypohidrosis 		disease Skin and Connective Tissue Diseases Disease or Syndrome 69 1 0.100 None 0
CUI: C0032617
Disease: Polyuria
Polyuria 		phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Sign or Symptom 73 3 0.100 None 0
CUI: C4023106
Disease: Obstructive azoospermia
Obstructive azoospermia 		disease Male Urogenital Diseases Disease or Syndrome 74 9 0.010 None 1.000 1 2010 2010
CUI: C0012739
Disease: Disseminated Intravascular Coagulation
Disseminated Intravascular Coagulation 		disease Hemic and Lymphatic Diseases Disease or Syndrome 117 3 0.010 None 1.000 1 2019 2019
CUI: C0027709
Disease: Nephrocalcinosis
Nephrocalcinosis 		disease Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 118 20 0.010 None 1.000 1 2018 2018
CUI: C1963094
Disease: Dry Skin, CTCAE
Dry Skin, CTCAE 		phenotype Finding 137 0.100 None 0
CUI: C0151908
Disease: Dry skin
Dry skin 		phenotype Skin and Connective Tissue Diseases Sign or Symptom 159 12 0.100 None 0