Ablepharon
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Congenital Abnormality
|
20
|
1
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Acantholysis
|
phenotype |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
|
Pathologic Function
|
11
|
|
0.100 |
None |
|
0 |
|
|
|
Acanthosis
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Finding
|
37
|
|
0.100 |
None |
|
0 |
|
|
|
Allergic Reaction
|
phenotype |
Immune System Diseases
|
Pathologic Function
|
197
|
1019
|
0.300 |
None |
1.000 |
1 |
|
2013 |
2013 |
CUI: |
C0860659 |
Disease: |
Aloof
|
Aloof
|
disease |
|
Mental or Behavioral Dysfunction
|
81
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Alzheimer's Disease
|
disease |
Nervous System Diseases; Mental Disorders
|
Disease or Syndrome
|
3397
|
1843
|
0.010 |
None |
1.000 |
1 |
|
2005 |
2005 |
Autoimmune Diseases
|
group |
Immune System Diseases
|
Disease or Syndrome
|
1758
|
428
|
0.040 |
None |
0.750 |
4 |
|
2002 |
2019 |
Autoimmune skin disease
|
disease |
Skin and Connective Tissue Diseases; Immune System Diseases
|
Disease or Syndrome
|
9
|
|
0.030 |
None |
1.000 |
3 |
|
2002 |
2019 |
Bicuspid aortic valve
|
disease |
Cardiovascular Diseases
|
Congenital Abnormality
|
154
|
23
|
0.100 |
None |
|
0 |
1
|
|
|
Bullous impetigo
|
disease |
Infections; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
5
|
|
0.020 |
None |
1.000 |
2 |
|
2009 |
2020 |
Bullous pemphigoid
|
disease |
Skin and Connective Tissue Diseases; Immune System Diseases
|
Disease or Syndrome
|
127
|
11
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
bullous staphylococcal impetigo
|
disease |
Infections; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
5
|
|
0.020 |
None |
1.000 |
2 |
|
2009 |
2020 |
Carcinogenesis
|
phenotype |
Pathological Conditions, Signs and Symptoms; Neoplasms
|
Neoplastic Process
|
6243
|
355
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Cardiomyopathies
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
925
|
294
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Complete Trisomy 21 Syndrome
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
669
|
77
|
0.010 |
None |
1.000 |
1 |
|
2005 |
2005 |
Crohn Disease
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
1382
|
1147
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Dentinogenesis Imperfecta
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
|
Congenital Abnormality
|
35
|
7
|
0.070 |
None |
1.000 |
7 |
|
1995 |
2010 |
Dermatitis
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
496
|
16
|
0.340 |
None |
1.000 |
4 |
|
2013 |
2019 |
Dermatitis, Atopic
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases
|
Disease or Syndrome
|
751
|
232
|
0.020 |
None |
1.000 |
2 |
|
2017 |
2017 |
Dermatologic disorders
|
group |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
617
|
21
|
0.100 |
None |
1.000 |
14 |
|
1997 |
2017 |
Diffuse palmoplantar hyperkeratosis
|
disease |
|
Disease or Syndrome
|
2
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
Diffuse palmoplantar keratoderma with painful fissures
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
1
|
|
0.300 |
None |
1.000 |
1 |
|
2005 |
2005 |
Disease of mucous membrane
|
group |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
30
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Down Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
766
|
80
|
0.010 |
None |
1.000 |
1 |
|
2005 |
2005 |
Eczema
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
863
|
368
|
0.020 |
None |
1.000 |
2 |
|
2017 |
2017 |