Superficial ulcer
|
disease |
Pathological Conditions, Signs and Symptoms
|
Acquired Abnormality
|
242
|
10
|
0.020 |
None |
0.500 |
2 |
|
2017 |
2018 |
Lymphatic Abnormalities
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Anatomical Abnormality
|
30
|
6
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Milium Cyst
|
disease |
Pathological Conditions, Signs and Symptoms; Neoplasms; Skin and Connective Tissue Diseases
|
Anatomical Abnormality
|
20
|
|
0.100 |
None |
|
0 |
|
|
|
Pterygium of nail
|
disease |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
|
Anatomical Abnormality
|
4
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
Generalized abnormality of skin
|
disease |
|
Anatomical Abnormality
|
3
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
Abnormality of skin morphology
|
phenotype |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Anatomical Abnormality
|
16
|
2
|
0.100 |
None |
|
0 |
1
|
|
|
Epidermolysis Bullosa
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Congenital Abnormality
|
47
|
3
|
0.100 |
None |
0.923 |
13 |
|
1997 |
2016 |
Junctional epidermolysis bullosa mitis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Congenital Abnormality
|
2
|
|
0.050 |
None |
1.000 |
5 |
|
1997 |
2001 |
Amelogenesis Imperfecta
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
|
Congenital Abnormality
|
61
|
24
|
0.330 |
strong |
1.000 |
4 |
1
|
1996 |
2016 |
Agenesis
|
disease |
|
Congenital Abnormality
|
161
|
44
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Congenital pyloric atresia
|
disease |
|
Congenital Abnormality
|
6
|
2
|
0.010 |
None |
1.000 |
1 |
|
1999 |
1999 |
Hypodontia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
|
Congenital Abnormality
|
218
|
48
|
0.100 |
None |
|
0 |
|
|
|
Skin Abnormalities
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Congenital Abnormality
|
106
|
16
|
0.100 |
None |
|
0 |
1
|
|
|
ANONYCHIA
|
disease |
Pathological Conditions, Signs and Symptoms
|
Congenital Abnormality
|
30
|
2
|
0.100 |
None |
|
0 |
|
|
|
Aplasia Cutis Congenita
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Congenital Abnormality
|
393
|
14
|
0.100 |
None |
|
0 |
|
|
|
Nail dysplasia
|
disease |
Pathological Conditions, Signs and Symptoms
|
Congenital Abnormality
|
78
|
2
|
0.100 |
None |
|
0 |
|
|
|
Bullous pemphigoid
|
disease |
Skin and Connective Tissue Diseases; Immune System Diseases
|
Disease or Syndrome
|
127
|
11
|
0.100 |
None |
0.978 |
93 |
|
1990 |
2020 |
Junctional Epidermolysis Bullosa
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
16
|
9
|
0.500 |
strong |
0.976 |
41 |
4
|
1995 |
2018 |
Adult junctional epidermolysis bullosa (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
6
|
35
|
0.700 |
strong |
1.000 |
16 |
13
|
1996 |
2014 |
Pemphigoid Gestationis
|
phenotype |
Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
8
|
|
0.100 |
None |
1.000 |
10 |
|
1990 |
2018 |
Dermatologic disorders
|
group |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
617
|
21
|
0.100 |
None |
1.000 |
10 |
|
1997 |
2019 |
Leukocyte adhesion deficiency type 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases
|
Disease or Syndrome
|
114
|
26
|
0.060 |
None |
1.000 |
6 |
|
2000 |
2014 |
Linear IgA Bullous Dermatosis
|
disease |
Skin and Connective Tissue Diseases; Immune System Diseases
|
Disease or Syndrome
|
4
|
|
0.060 |
None |
1.000 |
6 |
|
1997 |
2017 |
Epithelial Recurrent Erosion Dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
5
|
2
|
0.750 |
strong |
1.000 |
6 |
2
|
2003 |
2019 |
Autoimmune Diseases
|
group |
Immune System Diseases
|
Disease or Syndrome
|
1758
|
428
|
0.050 |
None |
1.000 |
5 |
|
1996 |
2019 |