NAVAJO NEUROHEPATOPATHY
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Nervous System Diseases
Disease or Syndrome
4
28
0.760
None
1.000
24
27
2006
2019
Depletion of mitochondrial DNA
disease
Disease or Syndrome
36
7
0.100
None
1.000
13
2006
2017
Deoxyguanosine Kinase Deficiency
disease
Nutritional and Metabolic Diseases
Disease or Syndrome
4
1
0.230
None
1.000
9
1990
2017
Liver Failure
disease
Digestive System Diseases
Disease or Syndrome
293
20
0.370
strong
1.000
8
2007
2019
Alport Syndrome, Autosomal Recessive
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases; Male Urogenital Diseases
Disease or Syndrome
8
2
0.200
None
1.000
6
1990
2009
Alport syndrome, recessive type
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases; Male Urogenital Diseases
Disease or Syndrome
3
0.200
None
1.000
6
1990
2009
ALPORT SYNDROME 2, AUTOSOMAL RECESSIVE
disease
Disease or Syndrome
4
143
0.200
None
1.000
6
1990
2009
Glomerulosclerosis (disorder)
disease
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases
Disease or Syndrome
221
3
0.040
None
1.000
4
1993
2004
SYMPHALANGISM, PROXIMAL
disease
Musculoskeletal Diseases
Disease or Syndrome
4
1
0.030
None
1.000
3
1995
2019
Cholestasis
disease
Digestive System Diseases
Disease or Syndrome
420
15
0.310
strong
1.000
2
2008
2014
Failure to Thrive
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
842
10
0.120
None
1.000
2
2017
2019
Mixed sensory-motor polyneuropathy
disease
Nervous System Diseases
Disease or Syndrome
20
8
0.020
None
1.000
2
2015
2019
Pediatric failure to thrive
disease
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Mental Disorders
Disease or Syndrome
166
122
0.020
None
1.000
2
2017
2019
Failure to thrive in infant
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
81
4
0.020
None
1.000
2
2017
2019
Amyloidosis
disease
Nutritional and Metabolic Diseases
Disease or Syndrome
694
93
0.010
None
< 0.001
1
2017
2017
Arteriosclerosis
disease
Cardiovascular Diseases
Disease or Syndrome
2006
267
0.010
None
1.000
1
2019
2019
Arthritis, Gouty
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Disease or Syndrome
206
2356
0.100
None
1.000
1
1
2013
2013
Myoclonic Epilepsy
disease
Nervous System Diseases
Disease or Syndrome
71
9
0.010
None
1.000
1
2018
2018
IGA Glomerulonephritis
disease
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases
Disease or Syndrome
456
130
0.010
None
1.000
1
2019
2019
Focal glomerulosclerosis
disease
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
281
50
0.310
None
1.000
1
2009
2009
×
CUI:
C0018099
Disease:
Gout
Gout
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Disease or Syndrome
205
2354
0.100
None
1.000
1
1
2013
2013
Incontinentia Pigmenti Achromians
disease
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
Congenital Abnormality
67
10
0.300
None
1.000
1
2009
2009
Leukodystrophy
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
Disease or Syndrome
190
27
0.010
None
1.000
1
2008
2008
Liver Cirrhosis
disease
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
Disease or Syndrome
1182
189
0.010
None
1.000
1
2009
2009
Kidney Failure
disease
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
378
36
0.010
None
1.000
1
2004
2004