Congenital rubella infection
|
disease |
|
Disease or Syndrome; Congenital Abnormality
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
2014 |
2014 |
Indirect Contact Transmission Infection
|
phenotype |
Pathological Conditions, Signs and Symptoms; Infections
|
Disease or Syndrome
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Disseminated cryptococcosis
|
disease |
Infections
|
Disease or Syndrome
|
2
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Rat Cholangiofibrosis
|
disease |
|
Disease or Syndrome
|
2
|
|
0.200 |
None |
1.000 |
1 |
|
2013 |
2013 |
Light Fixation Seizure Syndrome
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
|
Disease or Syndrome
|
3
|
|
0.040 |
None |
1.000 |
4 |
|
1993 |
2016 |
Congenital Rubella Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Infections
|
Disease or Syndrome
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
2000 |
2000 |
Subacute Combined Degeneration
|
disease |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
3
|
1
|
0.200 |
None |
1.000 |
1 |
|
2006 |
2006 |
HYPER-IgM IMMUNODEFICIENCY, X-LINKED, WITH ECTODERMAL DYSPLASIA, HYPOHIDROTIC
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
3
|
8
|
0.010 |
None |
1.000 |
1 |
|
2001 |
2001 |
Large tonsils (finding)
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Finding
|
3
|
|
0.100 |
None |
|
0 |
|
|
|
Impaired memory B cell generation
|
phenotype |
|
Cell or Molecular Dysfunction
|
3
|
|
0.100 |
None |
|
0 |
|
|
|
X-linked hypogammaglobulinemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
4
|
|
0.010 |
None |
1.000 |
1 |
|
1996 |
1996 |
Impaired Ig class switch recombination
|
phenotype |
|
Finding
|
4
|
|
0.100 |
None |
|
0 |
|
|
|
Absence of lymph node germinal center
|
phenotype |
|
Finding
|
4
|
|
0.100 |
None |
|
0 |
|
|
|
White Coat Hypertension
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
5
|
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Mycobacterium abscessus Infection
|
disease |
Infections
|
Disease or Syndrome
|
6
|
|
0.010 |
None |
1.000 |
1 |
|
2015 |
2015 |
Decreased T cell activation
|
phenotype |
|
Finding
|
6
|
|
0.100 |
None |
|
0 |
|
|
|
Post stroke epilepsy
|
disease |
|
Disease or Syndrome
|
7
|
2
|
0.010 |
None |
1.000 |
1 |
|
2014 |
2014 |
Immunoglobulin deficiency
|
disease |
Immune System Diseases
|
Disease or Syndrome
|
8
|
|
0.020 |
None |
1.000 |
2 |
|
1993 |
2018 |
Small Cell Lymphoma
|
disease |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
|
Neoplastic Process
|
8
|
|
0.010 |
None |
1.000 |
1 |
|
1975 |
1975 |
Immunodeficiency congenital
|
disease |
|
Disease or Syndrome; Congenital Abnormality
|
8
|
|
0.010 |
None |
1.000 |
1 |
|
2001 |
2001 |
Antisynthetase syndrome
|
disease |
Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
9
|
|
0.010 |
None |
1.000 |
1 |
|
2020 |
2020 |
Dysgammaglobulinemia
|
disease |
Immune System Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
10
|
|
0.110 |
None |
1.000 |
1 |
|
2000 |
2000 |
Autoimmune retinopathy
|
disease |
Eye Diseases; Immune System Diseases
|
Disease or Syndrome
|
10
|
|
0.010 |
None |
1.000 |
1 |
|
2005 |
2005 |
Hyperimmunoglobulin M syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
12
|
1
|
0.200 |
strong |
1.000 |
32 |
1
|
1993 |
2018 |
Bluetongue infection
|
disease |
Infections; Animal Diseases
|
Disease or Syndrome
|
13
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |