Prostate Cancer, Hereditary, 7
disease
Neoplasms; Male Urogenital Diseases
Neoplastic Process
59
11
0.010
None
1.000
1
2017
2017
Lymphedema
disease
Hemic and Lymphatic Diseases
Pathologic Function
61
1
0.400
None
1.000
1
2011
2011
Myeloid neoplasm
disease
Neoplasms; Hemic and Lymphatic Diseases
Neoplastic Process
62
5
0.010
None
1.000
1
2015
2015
Acquired aplastic anemia
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
64
12
0.020
None
1.000
2
2016
2016
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
0.030
None
1.000
3
2015
2015
Congenital neutropenia
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Congenital Abnormality
68
11
0.330
strong
1.000
4
2015
2018
Congenital sensorineural hearing loss
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
Congenital Abnormality
68
17
0.010
None
1.000
1
2018
2018
Myelodysplasia, CTCAE
phenotype
Finding
68
0.100
None
0
Dilatation of ureter
disease
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Anatomical Abnormality
72
2
0.020
None
1.000
2
2008
2019
Congenital deafness
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Nervous System Diseases; Otorhinolaryngologic Diseases
Congenital Abnormality
72
11
0.010
None
1.000
1
2018
2018
×
CUI:
C1968949
Disease:
Cakut
Cakut
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
72
8
0.010
None
1.000
1
2008
2008
Truncus Arteriosus, Persistent
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Congenital Abnormality
76
4
0.010
None
1.000
1
2012
2012
Li-Fraumeni Syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases
Disease or Syndrome
76
206
0.010
None
1.000
1
2019
2019
Opportunistic Infections
group
Infections
Disease or Syndrome
90
7
0.030
None
1.000
3
2013
2017
Cytogenetically normal acute myeloid leukemia
disease
Neoplasms
Neoplastic Process
91
9
0.020
None
1.000
2
2012
2014
Primary immune deficiency disorder
group
Immune System Diseases
Disease or Syndrome
93
23
0.010
None
1.000
1
2020
2020
Adult Teratoma
disease
Neoplasms
Neoplastic Process
93
3
0.010
None
1.000
1
2017
2017
Childhood Teratoma
disease
Neoplasms
Neoplastic Process
95
3
0.010
None
1.000
1
2017
2017
Cardiovascular Abnormalities
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Congenital Abnormality
99
12
0.300
None
1.000
1
2010
2010
Acute myelomonocytic leukemia
disease
Neoplasms
Neoplastic Process
105
3
0.020
None
1.000
2
2015
2018
Abnormal vision
phenotype
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
Finding
115
6
0.100
None
0
Lymphohistiocytosis, Hemophagocytic
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
117
13
0.010
None
1.000
1
2020
2020
Acute Undifferentiated Leukemia
disease
Neoplastic Process
119
1
0.010
None
1.000
1
2007
2007
Undifferentiated leukemia
disease
Neoplastic Process
120
2
0.010
None
1.000
1
2007
2007