Keratosis pilaris
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Acquired Abnormality
|
30
|
4
|
0.010 |
None |
1.000 |
1 |
|
1998 |
1998 |
Epithelial cyst
|
phenotype |
Neoplasms
|
Anatomical Abnormality
|
38
|
|
0.010 |
None |
1.000 |
1 |
|
1997 |
1997 |
Milium Cyst
|
disease |
Pathological Conditions, Signs and Symptoms; Neoplasms; Skin and Connective Tissue Diseases
|
Anatomical Abnormality
|
20
|
|
0.100 |
None |
|
0 |
|
|
|
Nail abnormality
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Anatomical Abnormality
|
67
|
11
|
0.100 |
None |
|
0 |
|
|
|
Abnormality of dental enamel
|
group |
|
Anatomical Abnormality
|
96
|
4
|
0.100 |
None |
|
0 |
|
|
|
Epidermolysis bullosa simplex with mottled pigmentation
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Congenital Abnormality
|
5
|
3
|
0.780 |
strong |
1.000 |
11 |
2
|
1996 |
2014 |
Epidermolysis Bullosa Simplex Kobner
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Congenital Abnormality
|
7
|
28
|
0.730 |
strong |
1.000 |
10 |
12
|
1993 |
2019 |
Epidermolysis Bullosa
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Congenital Abnormality
|
47
|
3
|
0.330 |
strong |
1.000 |
4 |
|
2006 |
2018 |
Congenital chromosomal disease
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
757
|
47
|
0.010 |
None |
< 0.001 |
1 |
|
2001 |
2001 |
Epidermolysis bullosa simplex herpetiformis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Congenital Abnormality
|
2
|
|
0.010 |
None |
1.000 |
1 |
|
1999 |
1999 |
Nail dysplasia
|
disease |
Pathological Conditions, Signs and Symptoms
|
Congenital Abnormality
|
78
|
2
|
0.100 |
None |
|
0 |
|
|
|
Epidermolysis Bullosa Simplex
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
30
|
33
|
0.900 |
strong |
0.985 |
68 |
16
|
1991 |
2019 |
Weber-Cockayne Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
4
|
42
|
0.760 |
strong |
1.000 |
18 |
25
|
1993 |
2019 |
Epidermolysis Bullosa Herpetiformis Dowling-Meara
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
4
|
29
|
0.950 |
strong |
1.000 |
16 |
15
|
1992 |
2019 |
dowling-degos disease
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
53
|
7
|
0.700 |
strong |
1.000 |
14 |
|
2006 |
2019 |
Dermatologic disorders
|
group |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
617
|
21
|
0.050 |
None |
1.000 |
5 |
|
2007 |
2019 |
Diabetes Mellitus
|
group |
Nutritional and Metabolic Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
2803
|
824
|
0.020 |
None |
1.000 |
2 |
|
2018 |
2018 |
Skin Diseases, Genetic
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
57
|
6
|
0.020 |
None |
1.000 |
2 |
|
2011 |
2011 |
Epidermolysis Bullosa Simplex with Migratory Circinate Erythema
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
2
|
3
|
0.620 |
None |
1.000 |
2 |
3
|
2003 |
2006 |
Basal epidermolysis bullosa simplex
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
2
|
|
0.020 |
None |
1.000 |
2 |
|
2010 |
2011 |
Acute pancreatitis
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
435
|
51
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Adrenal Gland Hyperfunction
|
phenotype |
Endocrine System Diseases
|
Disease or Syndrome
|
50
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Refractory anemias
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
340
|
11
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Rheumatoid Arthritis
|
disease |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases
|
Disease or Syndrome
|
2723
|
2387
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Atrioventricular Block
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
63
|
17
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |