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: C0017162
Disease: Gastroenteritis, Transmissible, of Swine
Gastroenteritis, Transmissible, of Swine 		disease Infections; Animal Diseases Disease or Syndrome 1 0.300 None 1.000 1 2017 2017
CUI: C4747974
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2DD
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2DD 		disease Disease or Syndrome 2 4 0.700 strong 1.000 2 4 2018 2018
CUI: C1706762
Disease: Aldosterone-Producing Adrenal Cortex Adenoma
Aldosterone-Producing Adrenal Cortex Adenoma 		disease Neoplasms; Endocrine System Diseases Neoplastic Process 2 6 0.100 None 0 3
CUI: C0264641
Disease: Endocrine hypertension
Endocrine hypertension 		disease Endocrine System Diseases; Cardiovascular Diseases Disease or Syndrome 4 0.010 None 1.000 1 2013 2013
CUI: C0424375
Disease: Biting self
Biting self 		phenotype Behavior and Behavior Mechanisms Finding 4 3 0.100 None 0
CUI: C1846348
Disease: Renal potassium wasting
Renal potassium wasting 		phenotype Finding 6 1 0.100 None 0
CUI: C0042594
Disease: Vestibular Diseases
Vestibular Diseases 		group Otorhinolaryngologic Diseases Disease or Syndrome 10 0.300 None 1.000 1 2011 2011
CUI: C1835171
Disease: Hypomagnesemia 2, renal
Hypomagnesemia 2, renal 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 10 1 0.100 None 0
CUI: C0018776
Disease: Hearing Loss, Central
Hearing Loss, Central 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 12 0.200 None 1.000 1 2014 2014
CUI: C3713420
Disease: Familial Hyperaldosteronism
Familial Hyperaldosteronism 		disease Endocrine System Diseases Disease or Syndrome 15 0.010 None 1.000 1 2016 2016
CUI: C4552839
Disease: Hypomagnesemia, CTCAE
Hypomagnesemia, CTCAE 		phenotype Finding 21 0.400 strong 1.000 1 2018 2018
CUI: C0155616
Disease: Secondary hypertension
Secondary hypertension 		disease Cardiovascular Diseases Disease or Syndrome 22 1 0.010 None 1.000 1 2013 2013
CUI: C0018780
Disease: Hearing Loss, High-Frequency
Hearing Loss, High-Frequency 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 35 8 0.200 None 1.000 1 2014 2014
CUI: C0205649
Disease: Adenoma, Monomorphic
Adenoma, Monomorphic 		disease Neoplasms Neoplastic Process 36 0.300 None 1.000 2 2013 2013
CUI: C0205651
Disease: Adenoma, Trabecular
Adenoma, Trabecular 		disease Neoplasms Neoplastic Process 37 0.300 None 1.000 2 2013 2013
CUI: C0205650
Disease: Papillary adenoma
Papillary adenoma 		disease Neoplasms Neoplastic Process 39 0.300 None 1.000 2 2013 2013
CUI: C0205648
Disease: Adenoma, Microcystic
Adenoma, Microcystic 		disease Neoplasms Neoplastic Process 45 0.300 None 1.000 2 2013 2013
CUI: C0205646
Disease: Adenoma, Basal Cell
Adenoma, Basal Cell 		disease Neoplasms Neoplastic Process 49 0.300 None 1.000 2 2013 2013
CUI: C0427149
Disease: Gait, Drop Foot
Gait, Drop Foot 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 51 5 0.100 None 0
CUI: C3694279
Disease: Middle East Respiratory Syndrome
Middle East Respiratory Syndrome 		disease Infections Disease or Syndrome 53 0.010 None 1.000 1 2015 2015
CUI: C0151723
Disease: Hypomagnesemia
Hypomagnesemia 		phenotype Nutritional and Metabolic Diseases Disease or Syndrome 58 11 0.420 strong 1.000 2 2018 2020
CUI: C0020621
Disease: Hypokalemia
Hypokalemia 		phenotype Nutritional and Metabolic Diseases Finding 61 7 0.100 None 0
CUI: C1866141
Disease: Foot dorsiflexor weakness
Foot dorsiflexor weakness 		phenotype Finding 70 4 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: C1384514
Disease: Conn Syndrome
Conn Syndrome 		disease Endocrine System Diseases Disease or Syndrome 82 25 0.320 None 1.000 3 2013 2019