Carcinoma breast stage IV
|
disease |
|
Neoplastic Process
|
573
|
14
|
0.010 |
None |
1.000 |
1 |
|
2012 |
2012 |
Impaired insulin secretion
|
disease |
|
Disease or Syndrome
|
88
|
14
|
0.010 |
None |
1.000 |
1 |
1
|
2003 |
2003 |
HER2-negative breast cancer
|
disease |
|
Neoplastic Process
|
160
|
18
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Cutaneous plaque
|
phenotype |
|
Finding
|
19
|
107
|
0.100 |
None |
|
0 |
|
|
|
Abnormal blistering of the skin
|
phenotype |
|
Finding
|
75
|
10
|
0.100 |
None |
|
0 |
|
|
|
Hypertensive disease
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
2322
|
1085
|
0.010 |
None |
1.000 |
1 |
1
|
2004 |
2004 |
Corneal dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
113
|
25
|
0.100 |
None |
|
0 |
|
|
|
ANOPHTHALMIA AND PULMONARY HYPOPLASIA
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Respiratory Tract Diseases
|
Disease or Syndrome
|
1410
|
80
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Hyperkeratosis of the palms and soles and esophageal papillomas
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
5
|
3
|
0.050 |
None |
1.000 |
5 |
1
|
1995 |
2013 |
PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
2
|
5
|
0.700 |
strong |
1.000 |
3 |
3
|
1995 |
2011 |
Pachyonychia Congenita
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
18
|
7
|
0.600 |
None |
1.000 |
18 |
1
|
2001 |
2020 |
Pachyonychia Congenita, Jadassohn Lewandowsky Type
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
8
|
19
|
0.950 |
strong |
1.000 |
13 |
12
|
1995 |
2013 |
Keratoderma, Palmoplantar, Diffuse
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
13
|
1
|
0.240 |
None |
1.000 |
5 |
|
1999 |
2017 |
PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
8
|
1
|
0.050 |
None |
1.000 |
5 |
|
1995 |
2017 |
Keratoderma, Palmoplantar
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
165
|
19
|
0.140 |
None |
1.000 |
4 |
|
2010 |
2020 |
Ichthyoses
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
194
|
18
|
0.110 |
None |
1.000 |
1 |
|
2017 |
2017 |
Congenital ichthyosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
80
|
11
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Keratosis Follicularis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
57
|
21
|
0.010 |
None |
1.000 |
1 |
|
1999 |
1999 |
Skin Diseases, Genetic
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
57
|
6
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Epidermolytic palmoplantar keratoderma of Vorner
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Congenital Abnormality
|
3
|
|
0.300 |
None |
1.000 |
1 |
|
1995 |
1995 |
Keratoderma, Palmoplantar, Epidermolytic
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
7
|
16
|
0.400 |
None |
1.000 |
1 |
|
1995 |
1995 |
Epidermolytic palmoplantar keratoderma Vorner type
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
3
|
|
0.300 |
None |
1.000 |
1 |
|
1995 |
1995 |
Keratosis Palmaris et Plantaris Familiaris
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
2
|
|
0.200 |
None |
1.000 |
1 |
|
2012 |
2012 |
Keratosis pilaris
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Acquired Abnormality
|
30
|
4
|
0.100 |
None |
|
0 |
|
|
|
Pachyonychia Congenita, Type 2 (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
5
|
13
|
0.500 |
None |
|
0 |
|
|
|