LYZ, lysozyme, 4069

N. diseases: 178; N. variants: 8
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: C0743746
Disease: eyes dry chronic
eyes dry chronic 		disease Disease or Syndrome 2 0.010 None 1.000 1 2018 2018
CUI: C0519002
Disease: Gastrointestinal amyloidosis
Gastrointestinal amyloidosis 		disease Nutritional and Metabolic Diseases Disease or Syndrome 3 1 0.020 None 1.000 2 2002 2017
CUI: C0232487
Disease: Abdominal discomfort
Abdominal discomfort 		phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Sign or Symptom 3 0.010 None 1.000 1 2012 2012
CUI: C0267537
Disease: Typhlitis
Typhlitis 		disease Digestive System Diseases; Infections Disease or Syndrome 4 0.010 None 1.000 1 2003 2003
CUI: C0268384
Disease: Familial Amyloid Neuropathy, Portuguese Type
Familial Amyloid Neuropathy, Portuguese Type 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 6 2 0.010 None 1.000 1 2012 2012
CUI: C1862968
Disease: Generalized amyloid deposition
Generalized amyloid deposition 		phenotype Nutritional and Metabolic Diseases Finding 6 0.100 None 0
CUI: C0268389
Disease: Amyloidosis, familial visceral
Amyloidosis, familial visceral 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 8 15 0.700 None 1.000 4 5 1991 2012
CUI: C0010930
Disease: Dacryocystitis
Dacryocystitis 		disease Eye Diseases Disease or Syndrome 8 0.010 None 1.000 1 2017 2017
CUI: C1334655
Disease: Mediastinal Germ Cell Tumor
Mediastinal Germ Cell Tumor 		disease Neoplasms; Respiratory Tract Diseases Neoplastic Process 8 2 0.010 None < 0.001 1 2006 2006
CUI: C0019624
Disease: Histiocytosis, Non-Langerhans-Cell
Histiocytosis, Non-Langerhans-Cell 		disease Hemic and Lymphatic Diseases Disease or Syndrome 9 2 0.010 None < 0.001 1 2019 2019
CUI: C0232491
Disease: Chronic abdominal pain
Chronic abdominal pain 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 9 0.010 None 1.000 1 2012 2012
CUI: C0399452
Disease: Supragingival dental plaque
Supragingival dental plaque 		disease Stomatognathic Diseases Disease or Syndrome 9 0.010 None 1.000 1 2001 2001
CUI: C4081731
Disease: Hereditary systemic amyloidosis
Hereditary systemic amyloidosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 10 6 0.090 None 1.000 9 3 1993 2019
CUI: C0031256
Disease: Petechiae
Petechiae 		disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases; Cardiovascular Diseases Disease or Syndrome 11 5 0.010 None 1.000 1 1 1999 1999
CUI: C0559469
Disease: Allergy to eggs
Allergy to eggs 		phenotype Immune System Diseases Disease or Syndrome 13 3 0.010 None 1.000 1 2018 2018
CUI: C3541517
Disease: ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT
ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT 		disease Disease or Syndrome 18 10 0.010 None 1.000 1 2016 2016
CUI: C3888065
Disease: ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT
ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT 		disease Disease or Syndrome 18 11 0.010 None 1.000 1 2016 2016
CUI: C0740340
Disease: Amyloidosis, Familial
Amyloidosis, Familial 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 19 12 0.050 None 0.800 5 3 2002 2019
CUI: C0268382
Disease: Amyloid nephropathy
Amyloid nephropathy 		disease Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 20 7 0.030 None 1.000 3 3 1994 2003
CUI: C0334347
Disease: Eccrine spiradenoma
Eccrine spiradenoma 		disease Neoplasms Neoplastic Process 20 0.010 None 1.000 1 1997 1997
CUI: C0268380
Disease: Systemic amyloidosis
Systemic amyloidosis 		disease Nutritional and Metabolic Diseases Disease or Syndrome 21 10 0.020 None 1.000 2 2003 2012
CUI: C0004059
Disease: aspirin intolerance
aspirin intolerance 		phenotype Sign or Symptom 23 4 0.010 None 1.000 1 2016 2016
CUI: C3539920
Disease: ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE
ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE 		disease Disease or Syndrome 25 7 0.010 None 1.000 1 2016 2016
CUI: C3887494
Disease: ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE
ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 25 35 0.010 None 1.000 1 2016 2016
CUI: C0281479
Disease: Primary Systemic Amyloidosis
Primary Systemic Amyloidosis 		disease Neoplasms; Nutritional and Metabolic Diseases; Immune System Diseases Neoplastic Process 27 10 0.020 None 1.000 2 2003 2012