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: C3825272
Disease: Food allergy in infants
Food allergy in infants 		disease Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C4024843
Disease: Late onset atopic dermatitis
Late onset atopic dermatitis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 2 0.010 None 1.000 1 2017 2017
CUI: C4025296
Disease: Brittle scalp hair
Brittle scalp hair 		phenotype Finding 2 0.100 None 0
CUI: C1850544
Disease: Hypernatremic dehydration
Hypernatremic dehydration 		phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Finding 3 0.100 None 0
CUI: C1299888
Disease: laminitis
laminitis 		disease Disease or Syndrome 4 0.010 None 1.000 1 2018 2018
CUI: C0236175
Disease: Increased IgE level
Increased IgE level 		phenotype Finding 4 6 0.100 None 0 2
CUI: C1840253
Disease: IgE RESPONSIVENESS, ATOPIC
IgE RESPONSIVENESS, ATOPIC 		disease Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome 5 0.300 strong 1.000 1 2002 2002
CUI: C0038165
Disease: Staphylococcal Scalded Skin Syndrome
Staphylococcal Scalded Skin Syndrome 		disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 7 0.010 None 1.000 1 2005 2005
CUI: C0263485
Disease: Clastothrix
Clastothrix 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 8 0.100 None 0
CUI: C0016470
Disease: Food Allergy
Food Allergy 		phenotype Immune System Diseases Pathologic Function 9 0.100 None 0
CUI: C0239816
Disease: Hand eczema
Hand eczema 		disease Skin and Connective Tissue Diseases Disease or Syndrome 17 8 0.020 None 1.000 2 1 2011 2012
CUI: C0002994
Disease: Angioedema
Angioedema 		phenotype Skin and Connective Tissue Diseases; Immune System Diseases; Cardiovascular Diseases Pathologic Function 18 8 0.100 None 0
CUI: C0267456
Disease: Villous atrophy of intestine
Villous atrophy of intestine 		disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 19 0.100 None 0
CUI: C0554101
Disease: Villous atrophy
Villous atrophy 		phenotype Finding 19 0.100 None 0
CUI: C0004059
Disease: aspirin intolerance
aspirin intolerance 		phenotype Sign or Symptom 23 4 0.010 None 1.000 1 2 2012 2012
CUI: C4021745
Disease: Abnormality of the musculature
Abnormality of the musculature 		phenotype Anatomical Abnormality 24 0.100 None 0
CUI: C0079583
Disease: Ichthyosiform Erythroderma, Congenital
Ichthyosiform Erythroderma, Congenital 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 31 11 0.030 None 1.000 3 2004 2008
CUI: C0030436
Disease: Parakeratosis
Parakeratosis 		disease Skin and Connective Tissue Diseases Disease or Syndrome 31 0.100 None 0
CUI: C0079154
Disease: Congenital Nonbullous Ichthyosiform Erythroderma
Congenital Nonbullous Ichthyosiform Erythroderma 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 36 16 0.110 None 1.000 1 2019 2019
CUI: C0745091
Disease: Hypereosinophilia
Hypereosinophilia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 39 4 0.110 None 1.000 1 2009 2009
CUI: C0238207
Disease: Ectopic kidney
Ectopic kidney 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 41 3 0.100 None 0
CUI: C0263490
Disease: Brittle hair
Brittle hair 		disease Disease or Syndrome 45 1 0.100 None 0
CUI: C0014179
Disease: Endometritis
Endometritis 		disease Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 46 2 0.010 None 1.000 1 2018 2018
CUI: C1860236
Disease: Irregular hyperpigmentation
Irregular hyperpigmentation 		phenotype Skin and Connective Tissue Diseases Finding 55 2 0.100 None 0
CUI: C0037277
Disease: Skin Diseases, Genetic
Skin Diseases, Genetic 		group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 57 6 0.010 None 1.000 1 2016 2016