Yellow/white lesions of the retina
|
phenotype |
|
Finding
|
4
|
|
0.100 |
None |
|
0 |
|
|
|
Yellow/white lesions of the macula
|
phenotype |
|
Finding
|
5
|
|
0.100 |
None |
|
0 |
|
|
|
Vitelliform-like macular lesions
|
phenotype |
|
Finding
|
4
|
|
0.100 |
None |
|
0 |
|
|
|
Vitelliform Macular Dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
74
|
120
|
0.430 |
None |
1.000 |
4 |
1
|
2011 |
2019 |
Visual Impairment
|
phenotype |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Finding
|
422
|
|
0.100 |
None |
|
0 |
|
|
|
Visual field defects
|
group |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Finding
|
47
|
1
|
0.100 |
None |
|
0 |
|
|
|
Visual field constriction
|
phenotype |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Finding
|
57
|
1
|
0.100 |
None |
|
0 |
|
|
|
Violence
|
phenotype |
|
Mental or Behavioral Dysfunction
|
70
|
6
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Usher Syndrome, Type I
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases
|
Disease or Syndrome
|
23
|
168
|
0.010 |
None |
1.000 |
1 |
|
2012 |
2012 |
Usher Syndrome
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases
|
Disease or Syndrome
|
68
|
74
|
0.010 |
None |
1.000 |
1 |
|
2012 |
2012 |
Tumor Cell Invasion
|
phenotype |
|
Neoplastic Process
|
6626
|
169
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Tuberculosis
|
disease |
Infections
|
Disease or Syndrome
|
1256
|
328
|
0.010 |
None |
1.000 |
1 |
|
2020 |
2020 |
Transitory tachypnea of newborn
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases
|
Disease or Syndrome
|
5
|
|
0.010 |
None |
1.000 |
1 |
|
2005 |
2005 |
Surfactant Dysfunction
|
disease |
Respiratory Tract Diseases
|
Disease or Syndrome
|
10
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Stargardt's disease
|
phenotype |
|
Disease or Syndrome
|
45
|
24
|
0.340 |
None |
1.000 |
4 |
|
2007 |
2016 |
STARGARDT DISEASE 1 (disorder)
|
disease |
|
Disease or Syndrome
|
23
|
317
|
0.320 |
None |
1.000 |
2 |
|
2007 |
2012 |
Slow decrease in visual acuity
|
phenotype |
|
Finding
|
27
|
3
|
0.100 |
None |
|
0 |
|
|
|
Shwachman syndrome
|
disease |
|
Disease or Syndrome
|
49
|
13
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Septicemia
|
disease |
Pathological Conditions, Signs and Symptoms; Infections
|
Disease or Syndrome
|
1285
|
141
|
0.020 |
None |
1.000 |
2 |
|
2019 |
2019 |
Sepsis
|
disease |
Pathological Conditions, Signs and Symptoms; Infections
|
Disease or Syndrome
|
1453
|
144
|
0.020 |
None |
1.000 |
2 |
|
2019 |
2019 |
Sensorineural Hearing Loss (disorder)
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
|
Disease or Syndrome
|
783
|
111
|
0.100 |
None |
|
0 |
|
|
|
Scotoma, Central
|
phenotype |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Finding
|
43
|
2
|
0.100 |
None |
|
0 |
|
|
|
Rod-Cone Dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
194
|
33
|
0.120 |
None |
1.000 |
2 |
3
|
1996 |
1998 |
Rod dystrophy
|
disease |
|
Disease or Syndrome
|
2
|
2
|
0.010 |
None |
1.000 |
1 |
2
|
1996 |
1996 |
Retinitis punctata albescens (disorder)
|
disease |
Eye Diseases
|
Disease or Syndrome
|
10
|
10
|
0.540 |
None |
1.000 |
4 |
1
|
1993 |
1997 |