MYELOPROLIFERATIVE/LYMPHOPROLIFERATIVE NEOPLASMS, FAMILIAL (MULTIPLE TYPES), SUSCEPTIBILITY TO
|
disease |
|
Finding
|
1
|
10
|
0.700 |
None |
1.000 |
3 |
10
|
2015 |
2016 |
Erythrodysplasia
|
phenotype |
|
Finding
|
1
|
|
0.100 |
None |
|
0 |
|
|
|
familial acute myeloid leukemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
Disease or Syndrome
|
4
|
|
0.010 |
None |
1.000 |
1 |
|
2015 |
2015 |
respiratory compensation
|
disease |
|
Disease or Syndrome
|
7
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Acute erythroleukemia - M6a subtype
|
disease |
Neoplasms; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
8
|
|
0.300 |
None |
1.000 |
1 |
|
2019 |
2019 |
Acute myeloid leukemia FAB-M6
|
disease |
Neoplasms; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
8
|
|
0.300 |
None |
1.000 |
1 |
|
2019 |
2019 |
Acute erythroleukemia - M6b subtype
|
disease |
Neoplasms; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
8
|
|
0.300 |
None |
1.000 |
1 |
|
2019 |
2019 |
Increased blood monocyte number
|
phenotype |
|
Laboratory or Test Result
|
8
|
|
0.100 |
None |
|
0 |
|
|
|
Acute erythroleukemia
|
disease |
Neoplasms; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
13
|
1
|
0.300 |
None |
1.000 |
1 |
|
2019 |
2019 |
Dental White Spot
|
disease |
Stomatognathic Diseases
|
Disease or Syndrome
|
22
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Asymptomatic bacteriuria
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases
|
Disease or Syndrome
|
23
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Common acute lymphoblastic leukemia
|
disease |
|
Neoplastic Process
|
43
|
|
0.010 |
None |
1.000 |
1 |
|
2002 |
2002 |
Monocytosis
|
disease |
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
61
|
3
|
0.100 |
None |
|
0 |
|
|
|
Myeloid neoplasm
|
disease |
Neoplasms; Hemic and Lymphatic Diseases
|
Neoplastic Process
|
62
|
5
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Bone marrow hypocellularity
|
phenotype |
|
Finding
|
64
|
5
|
0.100 |
None |
|
0 |
|
|
|
Severe congenital neutropenia
|
phenotype |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
66
|
26
|
0.300 |
strong |
1.000 |
1 |
|
2017 |
2017 |
Myelodysplasia, CTCAE
|
phenotype |
|
Finding
|
68
|
|
0.100 |
None |
|
0 |
|
|
|
Sexually Transmitted Diseases
|
group |
Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases
|
Disease or Syndrome
|
75
|
3
|
0.010 |
None |
1.000 |
1 |
|
1995 |
1995 |
Li-Fraumeni Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
76
|
206
|
0.020 |
None |
1.000 |
2 |
|
2016 |
2019 |
Syphilis
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases
|
Disease or Syndrome
|
80
|
3
|
0.020 |
None |
1.000 |
2 |
|
1995 |
2014 |
Heartburn
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
139
|
5
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Leukemia, Myelomonocytic, Chronic
|
disease |
Neoplasms; Hemic and Lymphatic Diseases
|
Neoplastic Process
|
158
|
28
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Myelodysplasia
|
disease |
|
Congenital Abnormality
|
181
|
4
|
0.110 |
None |
1.000 |
1 |
|
2019 |
2019 |
Miller Dieker syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
182
|
9
|
0.020 |
None |
1.000 |
2 |
|
2016 |
2019 |
Adult Myelodysplastic Syndrome
|
disease |
Hemic and Lymphatic Diseases
|
Neoplastic Process
|
332
|
20
|
0.020 |
None |
1.000 |
2 |
1
|
2017 |
2017 |