Dermatologic disorders
|
group |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
617
|
21
|
0.100 |
None |
1.000 |
15 |
|
2017 |
2020 |
Sentinel node (disorder)
|
disease |
|
Disease or Syndrome
|
130
|
5
|
0.100 |
None |
1.000 |
13 |
|
1999 |
2008 |
ALBINISM, OCULOCUTANEOUS, TYPE IB (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
1
|
24
|
0.720 |
None |
1.000 |
11 |
24
|
1990 |
2017 |
Oculocutaneous albinism type 2
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
11
|
58
|
0.090 |
None |
0.889 |
9 |
1
|
1987 |
2013 |
ALBINOIDISM, OCULOCUTANEOUS, AUTOSOMAL DOMINANT
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
54
|
6
|
0.090 |
None |
1.000 |
9 |
|
1987 |
2019 |
Parkinson Disease
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
2078
|
990
|
0.080 |
None |
1.000 |
8 |
|
2005 |
2019 |
Enzyme inhibition disorder
|
phenotype |
|
Disease or Syndrome
|
171
|
1
|
0.060 |
None |
1.000 |
6 |
|
2018 |
2019 |
Pigmentation Disorders
|
group |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
16
|
|
0.050 |
None |
1.000 |
5 |
|
2017 |
2019 |
Chloasma
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
25
|
|
0.040 |
None |
1.000 |
4 |
|
2017 |
2019 |
Kidney Failure, Acute
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
826
|
32
|
0.030 |
None |
1.000 |
3 |
|
2017 |
2018 |
Hermanski-Pudlak Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
70
|
59
|
0.030 |
None |
1.000 |
3 |
|
1999 |
2019 |
Ocular albinism, type I
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
38
|
24
|
0.030 |
None |
1.000 |
3 |
|
2011 |
2017 |
Neurodegenerative Disorders
|
group |
Nervous System Diseases
|
Disease or Syndrome
|
1515
|
85
|
0.030 |
None |
1.000 |
3 |
|
2018 |
2019 |
Skin Pigmentation Disorder
|
group |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
21
|
|
0.030 |
None |
1.000 |
3 |
|
2017 |
2019 |
Progressive cGVHD
|
disease |
|
Disease or Syndrome
|
384
|
40
|
0.030 |
None |
1.000 |
3 |
|
1996 |
2008 |
Alzheimer's Disease
|
disease |
Nervous System Diseases; Mental Disorders
|
Disease or Syndrome
|
3397
|
1843
|
0.020 |
None |
1.000 |
2 |
|
2019 |
2019 |
Autoimmune Diseases
|
group |
Immune System Diseases
|
Disease or Syndrome
|
1758
|
428
|
0.020 |
None |
1.000 |
2 |
|
1999 |
2005 |
Uveomeningoencephalitic Syndrome
|
disease |
Eye Diseases; Immune System Diseases; Nervous System Diseases
|
Disease or Syndrome
|
102
|
27
|
0.020 |
None |
1.000 |
2 |
|
2006 |
2007 |
Blindness
|
phenotype |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
393
|
34
|
0.020 |
None |
1.000 |
2 |
|
2011 |
2014 |
Primary congenital glaucoma
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
24
|
25
|
0.020 |
None |
1.000 |
2 |
|
2006 |
2007 |
ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS (disorder)
|
disease |
|
Disease or Syndrome
|
2
|
14
|
0.600 |
None |
1.000 |
2 |
13
|
1997 |
2017 |
Angina, Unstable
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
129
|
21
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Astigmatism
|
disease |
Eye Diseases
|
Disease or Syndrome
|
148
|
45
|
0.110 |
None |
1.000 |
1 |
|
2018 |
2018 |
Ataxia Telangiectasia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
384
|
698
|
0.010 |
None |
1.000 |
1 |
|
2008 |
2008 |
Chediak-Higashi Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Immune System Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
41
|
14
|
0.010 |
None |
1.000 |
1 |
|
1999 |
1999 |