Neurodegeneration with brain iron accumulation (NBIA)
disease
Nutritional and Metabolic Diseases; Nervous System Diseases
Disease or Syndrome
40
2
0.400
None
0.974
39
2005
2019
Dystonia Disorders
group
Nervous System Diseases
Disease or Syndrome
167
37
0.100
None
1.000
14
2003
2019
Neurodegenerative Disorders
group
Nervous System Diseases
Disease or Syndrome
1515
85
0.390
None
1.000
11
2005
2019
Movement Disorders
group
Nervous System Diseases
Disease or Syndrome
362
247
0.080
None
1.000
8
2006
2019
Infantile Neuroaxonal Dystrophy
disease
Nervous System Diseases
Disease or Syndrome
17
25
0.070
None
1.000
7
2004
2013
Degenerative polyarthritis
disease
Musculoskeletal Diseases
Disease or Syndrome
1827
247
0.040
None
0.750
4
2017
2018
HUNTINGTON DISEASE-LIKE 2
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
Disease or Syndrome
18
1
0.040
None
1.000
4
2005
2018
Acanthocytosis
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
8
0.030
None
0.667
3
2005
2015
Abetalipoproteinemia
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Disease or Syndrome
65
19
0.130
None
0.667
3
2005
2015
Chorea Acanthocytosis Syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Disease or Syndrome
29
5
0.030
None
1.000
3
2005
2018
Extrapyramidal sign
phenotype
Sign or Symptom
116
7
0.030
None
1.000
3
2008
2019
Ceruloplasmin deficiency
disease
Nutritional and Metabolic Diseases; Nervous System Diseases
Disease or Syndrome
8
51
0.020
None
1.000
2
2008
2018
Hypobetalipoproteinemias
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Disease or Syndrome
20
11
0.020
None
1.000
2
2011
2018
Psychiatric symptom
phenotype
Sign or Symptom
95
12
0.020
None
1.000
2
2003
2019
Hepatolenticular Degeneration
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Nervous System Diseases
Disease or Syndrome
146
349
0.020
None
1.000
2
2018
2019
Hallermann's Syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Disease or Syndrome
13
1
0.020
None
1.000
2
2004
2005
Schimke immunoosseous dysplasia
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Male Urogenital Diseases; Respiratory Tract Diseases; Immune System Diseases; Cardiovascular Diseases
Congenital Abnormality
21
19
0.020
None
1.000
2
2012
2017
Degenerative Diseases, Spinal Cord
group
Nervous System Diseases
Disease or Syndrome
40
0.300
None
1.000
2
2006
2007
×
CUI:
C0030193
Disease:
Pain
Pain
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
1554
196
0.020
None
1.000
2
2018
2019
Parkinson Disease
disease
Nervous System Diseases
Disease or Syndrome
2078
990
0.020
None
1.000
2
2005
2010
Degenerative Diseases, Central Nervous System
group
Nervous System Diseases
Disease or Syndrome
43
0.300
None
1.000
2
2006
2007
Childhood Glioblastoma
disease
Neoplasms
Neoplastic Process
2527
98
0.010
None
1.000
1
2011
2011
Eosinophilic esophagitis
disease
Digestive System Diseases; Immune System Diseases; Hemic and Lymphatic Diseases
Disease or Syndrome
183
40
0.010
None
1.000
1
2019
2019
Hypoplasia of corpus callosum
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Congenital Abnormality
385
49
0.010
None
1.000
1
2010
2010
Malignant neoplasm of prostate
disease
Neoplasms; Male Urogenital Diseases
Neoplastic Process
4502
1082
0.010
None
1.000
1
1999
1999