Precapillary pulmonary hypertension
|
disease |
Respiratory Tract Diseases
|
Disease or Syndrome
|
1
|
1
|
0.010 |
None |
1.000 |
1 |
1
|
2014 |
2014 |
Grip strength decreased
|
phenotype |
|
Sign or Symptom
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
2005 |
2005 |
DERMATITIS HERPETIFORMIS, FAMILIAL
|
disease |
Skin and Connective Tissue Diseases; Immune System Diseases
|
Disease or Syndrome
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Bronchitis in children
|
disease |
|
Disease or Syndrome
|
4
|
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Asiderotic anemia
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
5
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Myofascial Pain Syndromes
|
disease |
Musculoskeletal Diseases
|
Disease or Syndrome
|
5
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Angioma, Cavernous
|
disease |
Neoplasms; Hemic and Lymphatic Diseases; Cardiovascular Diseases
|
Neoplastic Process
|
9
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Waisman syndrome
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
|
Disease or Syndrome
|
10
|
4
|
0.010 |
None |
1.000 |
1 |
|
2012 |
2012 |
Acute glaucoma
|
disease |
|
Disease or Syndrome
|
11
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Embryo Loss
|
phenotype |
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications
|
Pathologic Function
|
11
|
|
0.010 |
None |
1.000 |
1 |
|
2004 |
2004 |
Trigeminal Neuralgia, Idiopathic
|
disease |
Nervous System Diseases; Stomatognathic Diseases
|
Disease or Syndrome
|
12
|
|
0.300 |
None |
1.000 |
1 |
|
2016 |
2016 |
Secondary Trigeminal Neuralgia
|
disease |
Nervous System Diseases; Stomatognathic Diseases
|
Disease or Syndrome
|
12
|
|
0.300 |
None |
1.000 |
1 |
|
2016 |
2016 |
Childhood Chronic Myelogenous Leukemia, BCR-ABL1 Positive
|
disease |
Neoplasms; Hemic and Lymphatic Diseases
|
Neoplastic Process
|
12
|
1
|
0.010 |
None |
1.000 |
1 |
|
2011 |
2011 |
FANCONI ANEMIA, COMPLEMENTATION GROUP F
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
13
|
6
|
0.010 |
None |
1.000 |
1 |
|
2012 |
2012 |
Adult-onset citrullinemia type 2
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
14
|
15
|
0.010 |
None |
1.000 |
1 |
|
2015 |
2015 |
Traumatic occlusion
|
disease |
|
Disease or Syndrome
|
15
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Pneumonia due to Klebsiella pneumoniae
|
disease |
Infections; Respiratory Tract Diseases
|
Disease or Syndrome
|
16
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Hyperkeratosis lenticularis perstans
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
18
|
11
|
0.010 |
None |
1.000 |
1 |
|
2000 |
2000 |
Intraocular Lymphoma
|
disease |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
|
Neoplastic Process
|
19
|
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Infection by human herpesvirus 6
|
disease |
Infections
|
Disease or Syndrome
|
19
|
|
0.010 |
None |
1.000 |
1 |
|
2012 |
2012 |
Apert syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
20
|
24
|
0.010 |
None |
1.000 |
1 |
|
2012 |
2012 |
insulin resistance in diabetes
|
disease |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
21
|
1
|
0.010 |
None |
1.000 |
1 |
|
2003 |
2003 |
Poikiloderma of Kindler
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Stomatognathic Diseases
|
Disease or Syndrome
|
21
|
25
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Nonketotic Hyperglycinemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
21
|
182
|
0.010 |
None |
< 0.001 |
1 |
|
2018 |
2018 |
Melanosis coli
|
disease |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
22
|
5
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |