Neuropathy
|
group |
Nervous System Diseases
|
Disease or Syndrome
|
484
|
110
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Ankle stiff
|
phenotype |
|
Sign or Symptom
|
2
|
|
0.010 |
None |
1.000 |
1 |
|
2020 |
2020 |
Retinal defect
|
phenotype |
Eye Diseases
|
Anatomical Abnormality
|
13
|
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Caffeine related disorders
|
group |
|
Mental or Behavioral Dysfunction
|
360
|
56
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Hyperactive behavior
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Mental or Behavioral Dysfunction
|
1263
|
112
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Dyskeratosis Congenita
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
58
|
146
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Atrophic iris
|
disease |
Eye Diseases
|
Disease or Syndrome
|
9
|
|
0.010 |
None |
1.000 |
1 |
|
2002 |
2002 |
AICARDI-GOUTIERES SYNDROME
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Nervous System Diseases
|
Disease or Syndrome
|
117
|
12
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Mixed anxiety and depressive disorder
|
disease |
Mental Disorders
|
Mental or Behavioral Dysfunction
|
146
|
13
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Behavioral syndrome associated with physiological disturbance and physical factors
|
disease |
Mental Disorders
|
Mental or Behavioral Dysfunction
|
8
|
2
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
inflammatory joint disease
|
disease |
|
Disease or Syndrome
|
33
|
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Liver carcinoma
|
disease |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
5725
|
942
|
0.010 |
None |
1.000 |
1 |
|
2003 |
2003 |
Ductal plate malformation
|
disease |
|
Congenital Abnormality
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
2000 |
2000 |
Amaurosis congenita of Leber, type 1
|
disease |
Eye Diseases
|
Disease or Syndrome
|
81
|
60
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Multiple Chronic Conditions
|
disease |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
929
|
42
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
360
|
194
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Pneumonitis
|
disease |
Infections; Respiratory Tract Diseases
|
Disease or Syndrome
|
697
|
13
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
beta^+^ Thalassemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
156
|
44
|
0.010 |
None |
1.000 |
1 |
|
1996 |
1996 |
Absence Seizures
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Disease or Syndrome
|
205
|
8
|
0.010 |
None |
1.000 |
1 |
|
2011 |
2011 |
Tubulointerstitial fibrosis
|
phenotype |
|
Disease or Syndrome
|
328
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Trichohepatoenteric Syndrome
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
424
|
28
|
0.010 |
None |
< 0.001 |
1 |
|
2002 |
2002 |
arthritis symptoms
|
disease |
|
Disease or Syndrome
|
9
|
|
0.010 |
None |
1.000 |
1 |
|
2015 |
2015 |
Infantile Severe Myoclonic Epilepsy
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
63
|
32
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Reflex Epilepsy, Audiogenic
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
31
|
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
57
|
43
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |