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
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
TRIGONOCEPHALY 2
disease
Congenital Abnormality
1
2
0.600
limited
1.000
2
2
2001
2011
HIV Infections
group
Infections; Immune System Diseases
Disease or Syndrome
807
142
0.010
None
1.000
1
1
2012
2012
Finding of body mass index
phenotype
Finding
88
252
0.100
None
1.000
1
1
2013
2013
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
Body mass index procedure
phenotype
Diagnostic Procedure
88
252
0.100
None
1.000
1
1
2013
2013
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
CHROMOSOME 9p DELETION SYNDROME
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
5
0.200
None
1.000
3
2004
2011
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
Bifid nose
disease
Respiratory Tract Diseases; Otorhinolaryngologic Diseases
Congenital Abnormality
9
0.620
limited
1.000
3
2011
2013
Other deletions of part of a chromosome
disease
Congenital Abnormality
2
0.200
None
1.000
3
2004
2011
9p partial monosomy syndrome
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
1
0.200
None
1.000
3
2004
2011
BNAR syndrome
disease
Disease or Syndrome
3
0.030
None
0.667
3
2011
2013
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
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
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
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
Congenital absence of kidney
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Congenital Abnormality
33
3
0.010
None
1.000
1
2011
2011
Bifid Nose, Autosomal Recessive
disease
Respiratory Tract Diseases; Otorhinolaryngologic Diseases
Congenital Abnormality
1
0.300
None
1.000
1
2013
2013
×
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
Anorectal Malformations
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
Anatomical Abnormality
112
6
0.010
None
1.000
1
2011
2011