Paraparesis, Spastic
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
75
|
37
|
0.310 |
strong |
1.000 |
3 |
|
2005 |
2013 |
Adrenal gland hypofunction
|
phenotype |
Endocrine System Diseases
|
Disease or Syndrome
|
90
|
10
|
0.310 |
strong |
1.000 |
3 |
|
2007 |
2013 |
Spastic Paraplegia, Hereditary
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
123
|
41
|
0.310 |
strong |
1.000 |
3 |
|
2007 |
2015 |
Adrenoleukodystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
294
|
116
|
1.000 |
definitive |
0.977 |
266 |
89
|
1981 |
2020 |
Adrenomyeloneuropathy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
38
|
2
|
0.600 |
definitive |
0.974 |
38 |
1
|
1984 |
2019 |
Neurodegenerative Disorders
|
group |
Nervous System Diseases
|
Disease or Syndrome
|
1515
|
85
|
0.100 |
None |
1.000 |
17 |
|
1996 |
2019 |
Cerebral Adrenoleukodystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
9
|
|
0.080 |
None |
1.000 |
8 |
|
2010 |
2019 |
Demyelinating Diseases
|
group |
Nervous System Diseases
|
Disease or Syndrome
|
156
|
5
|
0.060 |
None |
1.000 |
6 |
|
1998 |
2010 |
Diffuse Cerebral Sclerosis of Schilder
|
disease |
Immune System Diseases; Nervous System Diseases
|
Disease or Syndrome
|
4
|
|
0.200 |
None |
1.000 |
5 |
|
1997 |
2004 |
Liver diseases
|
group |
Digestive System Diseases
|
Disease or Syndrome
|
1019
|
100
|
0.050 |
None |
1.000 |
5 |
|
2013 |
2020 |
Non-alcoholic Fatty Liver Disease
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
1058
|
222
|
0.050 |
None |
1.000 |
5 |
|
2008 |
2019 |
Peroxisomal Disorders
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
25
|
1
|
0.050 |
None |
0.800 |
5 |
|
1999 |
2019 |
Adrenal cortical hypofunction
|
disease |
Endocrine System Diseases
|
Disease or Syndrome
|
52
|
5
|
0.030 |
None |
1.000 |
3 |
|
2006 |
2010 |
Hepatitis C
|
disease |
Digestive System Diseases; Infections
|
Disease or Syndrome
|
1768
|
347
|
0.030 |
None |
1.000 |
3 |
|
2000 |
2019 |
Liver carcinoma
|
disease |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
5725
|
942
|
0.030 |
None |
1.000 |
3 |
|
2008 |
2019 |
nervous system disorder
|
group |
Nervous System Diseases
|
Disease or Syndrome
|
977
|
39
|
0.030 |
None |
1.000 |
3 |
|
2001 |
2012 |
Inflammatory disorder
|
group |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
391
|
8
|
0.020 |
None |
1.000 |
2 |
|
2008 |
2009 |
Lupus Erythematosus, Systemic
|
disease |
Skin and Connective Tissue Diseases; Immune System Diseases
|
Disease or Syndrome
|
1883
|
1172
|
0.020 |
None |
1.000 |
2 |
|
2013 |
2014 |
End Stage Liver Disease
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
80
|
3
|
0.020 |
None |
1.000 |
2 |
|
2018 |
2020 |
Alcoholic Liver Diseases
|
group |
Digestive System Diseases; Chemically-Induced Disorders
|
Disease or Syndrome
|
195
|
20
|
0.020 |
None |
1.000 |
2 |
|
2000 |
2013 |
Carcinogenesis
|
phenotype |
Pathological Conditions, Signs and Symptoms; Neoplasms
|
Neoplastic Process
|
6243
|
355
|
0.020 |
None |
1.000 |
2 |
|
2003 |
2010 |
Lupus Nephritis
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases; Male Urogenital Diseases; Immune System Diseases
|
Disease or Syndrome
|
503
|
64
|
0.020 |
None |
1.000 |
2 |
|
2013 |
2018 |
Dysfunction adrenal
|
disease |
Endocrine System Diseases
|
Disease or Syndrome
|
2
|
|
0.020 |
None |
1.000 |
2 |
|
1997 |
2019 |
Zellweger Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nervous System Diseases
|
Disease or Syndrome
|
36
|
1
|
0.020 |
None |
1.000 |
2 |
|
1984 |
2013 |
Contiguous Abcd1-Dxs1375e Deletion Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Disease or Syndrome
|
2
|
|
0.310 |
None |
1.000 |
2 |
|
2002 |
2013 |