Maturation defect
|
phenotype |
|
Acquired Abnormality
|
43
|
2
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Plaque, Amyloid
|
disease |
Pathological Conditions, Signs and Symptoms
|
Acquired Abnormality
|
123
|
10
|
0.010 |
None |
1.000 |
1 |
|
2011 |
2011 |
Dwarfism
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
|
Congenital Abnormality
|
1261
|
77
|
0.100 |
None |
|
0 |
|
|
|
Severe Acute Respiratory Syndrome
|
disease |
Infections; Respiratory Tract Diseases
|
Disease or Syndrome
|
117
|
1
|
0.100 |
None |
1.000 |
27 |
|
2003 |
2018 |
Psoriasis
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
1308
|
705
|
0.100 |
None |
0.875 |
24 |
1
|
1999 |
2018 |
Hepatitis B
|
disease |
Digestive System Diseases; Infections
|
Disease or Syndrome
|
1449
|
519
|
0.100 |
None |
1.000 |
16 |
|
1992 |
2019 |
Middle East Respiratory Syndrome
|
disease |
Infections
|
Disease or Syndrome
|
53
|
|
0.100 |
None |
1.000 |
12 |
|
2013 |
2019 |
Dermatologic disorders
|
group |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
617
|
21
|
0.090 |
None |
1.000 |
9 |
1
|
2001 |
2020 |
Virus Diseases
|
group |
Infections
|
Disease or Syndrome
|
1471
|
42
|
0.090 |
None |
1.000 |
9 |
|
2002 |
2018 |
Psoriasis vulgaris
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
255
|
80
|
0.060 |
None |
0.833 |
6 |
|
1999 |
2006 |
PEELING SKIN SYNDROME
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
67
|
11
|
0.630 |
strong |
1.000 |
5 |
4
|
2010 |
2013 |
Hypotrichosis simplex
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
37
|
5
|
0.050 |
None |
1.000 |
5 |
1
|
2003 |
2020 |
Occult hepatitis B
|
disease |
|
Disease or Syndrome
|
14
|
|
0.040 |
None |
0.750 |
4 |
|
2013 |
2017 |
Rheumatoid Arthritis
|
disease |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases
|
Disease or Syndrome
|
2723
|
2387
|
0.120 |
None |
1.000 |
3 |
2
|
2002 |
2013 |
Hepatitis C
|
disease |
Digestive System Diseases; Infections
|
Disease or Syndrome
|
1768
|
347
|
0.030 |
None |
1.000 |
3 |
|
2010 |
2018 |
ENCEPHALITIS/ENCEPHALOPATHY, MILD, WITH REVERSIBLE MYELIN VACUOLIZATION
|
disease |
|
Disease or Syndrome
|
9
|
1
|
0.030 |
None |
1.000 |
3 |
|
2017 |
2019 |
Asthma
|
disease |
Respiratory Tract Diseases; Immune System Diseases
|
Disease or Syndrome
|
2096
|
1536
|
0.110 |
None |
1.000 |
2 |
1
|
2005 |
2017 |
Hepatitis A
|
disease |
Digestive System Diseases; Infections
|
Disease or Syndrome
|
451
|
27
|
0.020 |
None |
1.000 |
2 |
|
1996 |
2008 |
Leigh Disease
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
144
|
114
|
0.020 |
None |
1.000 |
2 |
|
2012 |
2016 |
Epidemic diarrhea
|
disease |
Digestive System Diseases; Infections
|
Disease or Syndrome
|
19
|
|
0.020 |
None |
1.000 |
2 |
|
2017 |
2018 |
Hypotrichosis Simplex of Scalp
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
3
|
2
|
0.700 |
strong |
1.000 |
2 |
2
|
2003 |
2012 |
Alopecia
|
disease |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
491
|
375
|
0.010 |
None |
1.000 |
1 |
|
2010 |
2010 |
Alzheimer's Disease
|
disease |
Nervous System Diseases; Mental Disorders
|
Disease or Syndrome
|
3397
|
1843
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Behcet Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
502
|
243
|
0.100 |
None |
1.000 |
1 |
2
|
2012 |
2012 |
Blood Coagulation Disorders
|
group |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
267
|
31
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |