IMMUNODEFICIENCY, COMMON VARIABLE, 12
|
disease |
|
Disease or Syndrome
|
1
|
6
|
0.400 |
strong |
1.000 |
3 |
6
|
2015 |
2018 |
Leukemia, Feline
|
disease |
Neoplasms; Infections; Animal Diseases
|
Neoplastic Process
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
2006 |
2006 |
Subungual keratoacanthoma
|
disease |
Skin and Connective Tissue Diseases
|
Neoplastic Process
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
2011 |
2011 |
Perceptual disturbance
|
disease |
Mental Disorders
|
Mental or Behavioral Dysfunction
|
5
|
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
Incipient Schizophrenia
|
disease |
Mental Disorders
|
Mental or Behavioral Dysfunction
|
6
|
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
Acute central serous chorioretinopathy
|
disease |
Infections; Eye Diseases
|
Disease or Syndrome
|
7
|
3
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Oxalosis
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
9
|
|
0.300 |
None |
1.000 |
1 |
|
2005 |
2005 |
Well-differentiated papillary mesothelioma
|
disease |
Neoplasms
|
Neoplastic Process
|
9
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Ocular Adnexal Lymphoma
|
disease |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
|
Neoplastic Process
|
9
|
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Prodrome
|
phenotype |
|
Sign or Symptom
|
10
|
|
0.010 |
None |
1.000 |
1 |
|
2004 |
2004 |
Ectodermal dysplasia, hypohidrotic, with immune deficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases
|
Disease or Syndrome
|
10
|
13
|
0.010 |
None |
1.000 |
1 |
|
2008 |
2008 |
Immunoglobulin Deficiency, Late-Onset
|
disease |
Immune System Diseases
|
Disease or Syndrome
|
11
|
|
0.300 |
None |
|
0 |
|
|
|
Hyperplastic lymph node
|
disease |
|
Acquired Abnormality
|
12
|
|
0.010 |
None |
< 0.001 |
1 |
|
1991 |
1991 |
Posterior pharyngeal cleft
|
phenotype |
|
Finding
|
12
|
|
0.100 |
None |
|
0 |
|
|
|
Infantile malignant osteopetrosis
|
disease |
Musculoskeletal Diseases
|
Congenital Abnormality
|
13
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Adenomatoid Tumor
|
disease |
Neoplasms
|
Neoplastic Process
|
14
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Hyaline Membrane Disease
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases
|
Disease or Syndrome
|
15
|
|
0.010 |
None |
1.000 |
1 |
|
2005 |
2005 |
soft neurological signs
|
phenotype |
|
Sign or Symptom
|
15
|
1
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
Prodromal Symptoms
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
15
|
4
|
0.010 |
None |
1.000 |
1 |
|
2004 |
2004 |
Bronchiolitis, Viral
|
disease |
Infections; Respiratory Tract Diseases
|
Disease or Syndrome
|
16
|
|
0.010 |
None |
1.000 |
1 |
|
2016 |
2016 |
Recurrent sinopulmonary infections
|
phenotype |
|
Finding
|
16
|
|
0.400 |
strong |
1.000 |
1 |
|
2015 |
2015 |
Familial erythrocytosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
17
|
2
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
Schizoaffective disorder, bipolar type
|
disease |
Mental Disorders
|
Mental or Behavioral Dysfunction
|
17
|
10
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
Inflammatory disease of mucous membrane
|
group |
Digestive System Diseases; Stomatognathic Diseases
|
Pathologic Function
|
18
|
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
TIBIAL MUSCULAR DYSTROPHY, TARDIVE
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
18
|
18
|
0.010 |
None |
1.000 |
1 |
|
2001 |
2001 |