Acrokeratosis Verruciformis of Hopf
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome; Congenital Abnormality
|
1
|
2
|
0.740 |
None |
1.000 |
6 |
2
|
2003 |
2017 |
Darier Disease, Segmental
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
1
|
2
|
0.130 |
None |
1.000 |
3 |
2
|
2000 |
2011 |
Acantholytic Dyskeratotic Epidermal Nevus
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Neoplastic Process
|
1
|
|
0.300 |
None |
1.000 |
2 |
|
2006 |
2010 |
Darier Disease, Acral Hemorrhagic Type
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
1
|
2
|
0.100 |
None |
|
0 |
2
|
|
|
Subungual hyperkeratotic fragments
|
phenotype |
|
Finding
|
1
|
|
0.100 |
None |
|
0 |
|
|
|
Anal mucosal leukoplakia
|
phenotype |
|
Finding
|
2
|
|
0.100 |
None |
|
0 |
|
|
|
Acrokeratosis
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
3
|
|
0.100 |
None |
|
0 |
|
|
|
Hibernation, Myocardial
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
4
|
|
0.300 |
None |
1.000 |
1 |
|
2006 |
2006 |
Palmar pit
|
phenotype |
|
Finding
|
4
|
|
0.100 |
None |
|
0 |
|
|
|
Plantar pits
|
phenotype |
|
Finding
|
4
|
|
0.100 |
None |
|
0 |
|
|
|
Stunned Myocardium
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
5
|
|
0.300 |
None |
1.000 |
1 |
|
2006 |
2006 |
Major psychiatric illness
|
disease |
|
Mental or Behavioral Dysfunction
|
5
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Myocardial Stunning
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
6
|
|
0.300 |
None |
1.000 |
1 |
|
2006 |
2006 |
Hypertrophy of parotid gland
|
disease |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Stomatognathic Diseases
|
Disease or Syndrome
|
7
|
|
0.100 |
None |
|
0 |
|
|
|
Euthyroid Sick Syndromes
|
disease |
Endocrine System Diseases
|
Disease or Syndrome
|
9
|
1
|
0.200 |
None |
1.000 |
1 |
|
2017 |
2017 |
Acantholysis
|
phenotype |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
|
Pathologic Function
|
11
|
|
0.100 |
None |
|
0 |
|
|
|
Skin Vesicle
|
phenotype |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
|
Finding
|
20
|
|
0.100 |
None |
|
0 |
|
|
|
Adult Diffuse Astrocytoma
|
disease |
Neoplasms
|
Neoplastic Process
|
21
|
2
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Childhood Diffuse Astrocytoma
|
disease |
Neoplasms
|
Neoplastic Process
|
21
|
2
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Squamous Cell Neoplasms
|
group |
Neoplasms
|
Neoplastic Process
|
22
|
|
0.010 |
None |
1.000 |
1 |
|
2010 |
2010 |
Ridged nails
|
phenotype |
|
Finding
|
22
|
|
0.100 |
None |
|
0 |
|
|
|
Wolfram Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Eye Diseases; Male Urogenital Diseases; Nervous System Diseases; Endocrine System Diseases; Otorhinolaryngologic Diseases
|
Disease or Syndrome
|
28
|
7
|
0.010 |
None |
1.000 |
1 |
|
2001 |
2001 |
Parakeratosis
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
31
|
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
22q11 Deletion Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
31
|
2
|
0.010 |
None |
1.000 |
1 |
|
2012 |
2012 |
Bone Cysts
|
disease |
Neoplasms; Musculoskeletal Diseases
|
Anatomical Abnormality
|
35
|
4
|
0.010 |
None |
1.000 |
1 |
|
2009 |
2009 |