9p partial monosomy syndrome
|
disease |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
1
|
|
0.200 |
None |
1.000 |
3 |
|
2004 |
2011 |
Abnormal hair pattern
|
disease |
|
Anatomical Abnormality
|
15
|
1
|
0.100 |
None |
|
0 |
|
|
|
Abnormal respiratory system morphology
|
phenotype |
|
Anatomical Abnormality
|
1
|
|
0.100 |
None |
|
0 |
|
|
|
Abnormality of the 5th toe
|
phenotype |
|
Anatomical Abnormality
|
1
|
|
0.100 |
None |
|
0 |
|
|
|
Acrocephaly
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
35
|
|
0.300 |
None |
|
0 |
|
|
|
Anal Stenosis, CTCAE
|
phenotype |
|
Finding
|
27
|
|
0.100 |
None |
|
0 |
|
|
|
Anophthalmos
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Congenital Abnormality
|
89
|
6
|
0.100 |
None |
|
0 |
|
|
|
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 |
Anteriorly placed anus
|
phenotype |
|
Finding
|
34
|
5
|
0.100 |
None |
|
0 |
|
|
|
Anus Prolapse
|
disease |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
|
Acquired Abnormality
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
2011 |
2011 |
Bifid nasal tip
|
phenotype |
|
Finding
|
10
|
|
0.100 |
None |
|
0 |
|
|
|
Bifid nose
|
disease |
Respiratory Tract Diseases; Otorhinolaryngologic Diseases
|
Congenital Abnormality
|
9
|
|
0.620 |
limited |
1.000 |
3 |
|
2011 |
2013 |
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 |
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 |
BNAR syndrome
|
disease |
|
Disease or Syndrome
|
3
|
|
0.030 |
None |
0.667 |
3 |
|
2011 |
2013 |
Body mass index
|
phenotype |
|
Clinical Attribute
|
1014
|
2689
|
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 |
Brachycephaly
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
186
|
20
|
0.300 |
None |
|
0 |
|
|
|
Bulbous nose
|
phenotype |
|
Finding
|
123
|
13
|
0.100 |
None |
|
0 |
|
|
|
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 |
Cardiovascular Diseases
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
1756
|
711
|
0.100 |
None |
1.000 |
1 |
1
|
2019 |
2019 |
CHROMOSOME 9p DELETION SYNDROME
|
disease |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
5
|
|
0.200 |
None |
1.000 |
3 |
|
2004 |
2011 |
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 |
Coloboma of superior eyelid
|
phenotype |
|
Disease or Syndrome
|
6
|
|
0.100 |
None |
|
0 |
|
|
|