Wiskott-Aldrich Syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases
Disease or Syndrome
95
34
1.000
definitive
0.987
156
30
1994
2020
THROMBOCYTOPENIA 1 (disorder)
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Disease or Syndrome
30
18
0.800
strong
1.000
68
16
1995
2019
Neutropenia, Severe Congenital, X-Linked
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Disease or Syndrome
4
14
0.710
strong
1.000
34
12
1995
2017
Lymphoma
group
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
Neoplastic Process
1548
91
0.610
strong
1.000
2
2017
2019
Congenital neutropenia
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Congenital Abnormality
68
11
0.320
strong
1.000
2
1
2006
2018
Thrombocytopenia
phenotype
Hemic and Lymphatic Diseases
Disease or Syndrome
592
110
0.200
None
1.000
11
1
2002
2019
IGA Glomerulonephritis
disease
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases
Disease or Syndrome
456
130
0.200
None
1.000
1
2012
2012
Neutropenia
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
389
97
0.160
None
1.000
6
1
2002
2018
Immunologic Deficiency Syndromes
group
Immune System Diseases
Disease or Syndrome
973
31
0.140
None
1.000
4
2005
2018
Congenital thrombocytopenia
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases
Disease or Syndrome
19
3
0.130
None
1.000
3
1995
2015
Eczema
disease
Skin and Connective Tissue Diseases
Disease or Syndrome
863
368
0.130
None
1.000
3
2004
2014
Arthritis
disease
Musculoskeletal Diseases
Disease or Syndrome
1072
69
0.120
None
1.000
2
2014
2015
×
CUI:
C0015967
Disease:
Fever
Fever
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
1021
66
0.110
None
1.000
1
2017
2017
Marijuana Abuse
disease
Chemically-Induced Disorders; Mental Disorders
Mental or Behavioral Dysfunction
156
23
0.100
None
0.957
69
2005
2020
Cannabis use
disease
Mental or Behavioral Dysfunction
74
44
0.100
None
0.900
10
1975
2020
Sinusitis
disease
Infections; Respiratory Tract Diseases; Otorhinolaryngologic Diseases
Disease or Syndrome
97
0.100
None
0
Abnormal platelet function
phenotype
Finding
21
2
0.100
None
0
Pneumonia
disease
Infections; Respiratory Tract Diseases
Disease or Syndrome
1032
33
0.100
None
0
Abnormal eosinophil morphology
phenotype
Finding
3
0.100
None
0
Skin Abnormalities
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
Congenital Abnormality
106
16
0.100
None
0
Skin Ulcer
phenotype
Skin and Connective Tissue Diseases
Disease or Syndrome
151
1
0.100
None
0
Congenital hypoplasia of thymus
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormality
34
0.100
None
0
Decreased mean platelet volume
phenotype
Laboratory or Test Result
3
0.100
None
0
X- linked recessive
phenotype
Finding
172
1
0.100
None
0
Chronic diarrhea
disease
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
Disease or Syndrome
62
9
0.100
None
0