Pachyonychia Congenita, Type 2 (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
5
|
13
|
0.780 |
None |
1.000 |
23 |
13
|
1994 |
2013 |
Steatocystoma multiplex
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Neoplastic Process
|
3
|
4
|
0.750 |
strong |
1.000 |
7 |
4
|
1997 |
2019 |
Pachyonychia Congenita
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
18
|
7
|
0.700 |
None |
1.000 |
13 |
1
|
1995 |
2020 |
Skin Neoplasms
|
group |
Neoplasms; Skin and Connective Tissue Diseases
|
Neoplastic Process
|
363
|
9
|
0.320 |
None |
1.000 |
3 |
|
2015 |
2018 |
Squamous cell carcinoma of esophagus
|
disease |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
2053
|
329
|
0.310 |
None |
1.000 |
2 |
|
2011 |
2020 |
Malignant neoplasm of skin
|
disease |
Neoplasms; Skin and Connective Tissue Diseases
|
Neoplastic Process
|
508
|
38
|
0.300 |
None |
1.000 |
1 |
|
2015 |
2015 |
Carcinoma, Basal Cell
|
disease |
Neoplasms
|
Neoplastic Process
|
557
|
91
|
0.300 |
None |
1.000 |
1 |
|
2010 |
2010 |
Pigmented Basal Cell Carcinoma
|
disease |
Neoplasms
|
Neoplastic Process
|
28
|
|
0.300 |
None |
1.000 |
1 |
|
2010 |
2010 |
Sebocystomatosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
1
|
|
0.300 |
None |
1.000 |
1 |
|
2015 |
2015 |
Chloracne
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
38
|
|
0.300 |
None |
1.000 |
1 |
|
2011 |
2011 |
Pachyonychia Congenita, Jadassohn Lewandowsky Type
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
8
|
19
|
0.300 |
None |
|
0 |
|
|
|
Dystrophia unguium
|
disease |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
81
|
9
|
0.110 |
None |
1.000 |
1 |
|
1998 |
1998 |
Keratoderma, Palmoplantar
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
165
|
19
|
0.110 |
None |
1.000 |
1 |
|
2010 |
2010 |
Epithelial cyst
|
phenotype |
Neoplasms
|
Anatomical Abnormality
|
38
|
|
0.110 |
None |
1.000 |
1 |
|
2003 |
2003 |
Neoplasms
|
group |
Neoplasms
|
Neoplastic Process
|
10161
|
1644
|
0.100 |
None |
1.000 |
15 |
|
2015 |
2019 |
Psoriasis
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
1308
|
705
|
0.100 |
None |
0.929 |
14 |
|
2005 |
2019 |
Cataract
|
disease |
Eye Diseases
|
Acquired Abnormality
|
878
|
124
|
0.100 |
None |
|
0 |
|
|
|
Cutaneous plaque
|
phenotype |
|
Finding
|
19
|
107
|
0.100 |
None |
|
0 |
|
|
|
Subungual hyperkeratosis
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
5
|
|
0.100 |
None |
|
0 |
|
|
|
Respiratory Insufficiency
|
phenotype |
Respiratory Tract Diseases
|
Pathologic Function
|
315
|
15
|
0.100 |
None |
|
0 |
|
|
|
Onychogryposis
|
disease |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
17
|
|
0.100 |
None |
|
0 |
|
|
|
Laryngomalacia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Respiratory Tract Diseases; Otorhinolaryngologic Diseases
|
Congenital Abnormality
|
67
|
18
|
0.100 |
None |
|
0 |
|
|
|
Fibrous skin tumor of tuberous sclerosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases
|
Neoplastic Process
|
20
|
2
|
0.100 |
None |
|
0 |
|
|
|
Sparse and thin eyebrow
|
phenotype |
|
Finding
|
68
|
8
|
0.100 |
None |
|
0 |
|
|
|
Abnormality of nail color
|
disease |
Pathological Conditions, Signs and Symptoms
|
Finding
|
8
|
|
0.100 |
None |
|
0 |
|
|
|