Primary Myelofibrosis
disease
Hemic and Lymphatic Diseases
Neoplastic Process
282
29
0.010
None
1.000
1
2019
2019
Body mass index
phenotype
Clinical Attribute
1014
2689
0.100
None
1.000
1
1
2019
2019
Cardiovascular Diseases
group
Cardiovascular Diseases
Disease or Syndrome
1756
711
0.100
None
1.000
1
1
2019
2019
Cryptophthalmos syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Eye Diseases; Musculoskeletal Diseases; Male Urogenital Diseases
Disease or Syndrome
8
5
0.240
None
1.000
4
2011
2018
Congenital diaphragmatic hernia
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormality
239
31
0.320
None
1.000
3
2013
2018
Marles Greenberg Persaud syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Musculoskeletal Diseases
Disease or Syndrome
3
3
0.750
None
0.875
8
3
2001
2017
Diaphragmatic Hernia
phenotype
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
78
3
0.210
None
1.000
3
2013
2016
Congenital hernia of foramen of Morgagni
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormality
19
0.300
None
1.000
2
2013
2016
Congenital hernia of foramen of Bochdalek
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormality
21
0.300
None
1.000
2
2013
2016
Bifid Nose With Or Without Anorectal And Renal Anomalies
disease
Digestive System Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
1
2
0.720
None
0.800
5
2
2001
2014
Unilateral agenesis of kidney
disease
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Congenital Abnormality
69
7
0.300
None
1.000
2
2010
2014
×
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
2014
2014
Bifid nose
disease
Respiratory Tract Diseases; Otorhinolaryngologic Diseases
Congenital Abnormality
9
0.620
limited
1.000
3
2011
2013
BNAR syndrome
disease
Disease or Syndrome
3
0.030
None
0.667
3
2011
2013
Congenital absence of kidneys syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
110
0.410
None
1.000
2
2011
2013
Eye Abnormalities
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Congenital Abnormality
55
3
0.300
None
1.000
1
2013
2013
Body mass index procedure
phenotype
Diagnostic Procedure
88
252
0.100
None
1.000
1
1
2013
2013
Coloboma of eyelid
phenotype
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Disease or Syndrome
28
0.110
None
1.000
1
2013
2013
Bifid Nose, Autosomal Dominant
disease
Respiratory Tract Diseases; Otorhinolaryngologic Diseases
Disease or Syndrome
1
0.300
None
1.000
1
2013
2013
Bifid Nose, Autosomal Recessive
disease
Respiratory Tract Diseases; Otorhinolaryngologic Diseases
Congenital Abnormality
1
0.300
None
1.000
1
2013
2013
Finding of body mass index
phenotype
Finding
88
252
0.100
None
1.000
1
1
2013
2013
HIV Infections
group
Infections; Immune System Diseases
Disease or Syndrome
807
142
0.010
None
1.000
1
1
2012
2012
HIV-1 infection
disease
Disease or Syndrome
695
94
0.010
None
1.000
1
2012
2012
Other deletions of part of a chromosome
disease
Congenital Abnormality
2
0.200
None
1.000
3
2004
2011
CHROMOSOME 9p DELETION SYNDROME
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
5
0.200
None
1.000
3
2004
2011