Retinitis Pigmentosa 14
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
2
|
11
|
0.910 |
None |
1.000 |
8 |
11
|
1997 |
2010 |
Autosomal recessive retinitis pigmentosa
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Congenital Abnormality
|
82
|
31
|
0.080 |
None |
1.000 |
8 |
1
|
1998 |
2014 |
Amaurosis congenita of Leber, type 1
|
disease |
Eye Diseases
|
Disease or Syndrome
|
81
|
60
|
0.140 |
None |
1.000 |
5 |
2
|
2007 |
2017 |
Retinal Diseases
|
group |
Eye Diseases
|
Disease or Syndrome
|
714
|
56
|
0.130 |
None |
1.000 |
3 |
|
2007 |
2016 |
LEBER CONGENITAL AMAUROSIS 15
|
disease |
|
Disease or Syndrome
|
1
|
4
|
0.700 |
None |
1.000 |
2 |
4
|
2004 |
2007 |
Hereditary retinal dystrophy
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
42
|
1
|
0.200 |
None |
1.000 |
2 |
|
2000 |
2001 |
Obesity
|
disease |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
2821
|
1111
|
0.120 |
None |
1.000 |
2 |
|
1998 |
2000 |
Rod-Cone Dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
194
|
33
|
0.120 |
None |
1.000 |
2 |
1
|
1997 |
2015 |
Congenital nystagmus
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases
|
Congenital Abnormality
|
15
|
5
|
0.100 |
None |
1.000 |
1 |
1
|
2017 |
2017 |
Atrophoderma maculatum
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
39
|
2
|
0.100 |
None |
1.000 |
1 |
1
|
2017 |
2017 |
Intrauterine retardation
|
phenotype |
|
Pathologic Function
|
41
|
56
|
0.100 |
None |
1.000 |
1 |
1
|
2017 |
2017 |
Abnormality of retinal pigmentation
|
phenotype |
|
Finding
|
215
|
5
|
0.100 |
None |
1.000 |
1 |
1
|
2017 |
2017 |
Unspecified visual loss
|
phenotype |
Pathological Conditions, Signs and Symptoms; Eye Diseases
|
Sign or Symptom
|
235
|
11
|
0.010 |
None |
1.000 |
1 |
|
2014 |
2014 |
Small for gestational age (disorder)
|
phenotype |
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications
|
Finding
|
181
|
34
|
0.100 |
None |
1.000 |
1 |
1
|
2017 |
2017 |
Cancer-Associated Retinopathy
|
disease |
Neoplasms; Eye Diseases
|
Disease or Syndrome
|
6
|
|
0.010 |
None |
1.000 |
1 |
|
2000 |
2000 |
Severe visual impairment
|
disease |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
35
|
9
|
0.100 |
None |
1.000 |
1 |
1
|
2017 |
2017 |
Atrophic macular change
|
phenotype |
|
Finding
|
24
|
1
|
0.100 |
None |
1.000 |
1 |
1
|
2017 |
2017 |
Blindness
|
phenotype |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
393
|
34
|
0.110 |
None |
1.000 |
1 |
|
2007 |
2007 |
Electroretinogram abnormal
|
phenotype |
|
Finding
|
158
|
10
|
0.100 |
None |
1.000 |
1 |
1
|
2017 |
2017 |
Cone dysfunction syndrome
|
disease |
|
Disease or Syndrome
|
25
|
2
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Central topographic island
|
disease |
|
Disease or Syndrome
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
2014 |
2014 |
Photoreceptor degeneration
|
disease |
Eye Diseases
|
Disease or Syndrome
|
136
|
16
|
0.010 |
None |
1.000 |
1 |
|
2014 |
2014 |
Optic Neuropathy
|
disease |
Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
54
|
8
|
0.010 |
None |
1.000 |
1 |
|
2016 |
2016 |
Hepatitis C
|
disease |
Digestive System Diseases; Infections
|
Disease or Syndrome
|
1768
|
347
|
0.010 |
None |
1.000 |
1 |
|
2016 |
2016 |
Hepatitis C, Chronic
|
disease |
Digestive System Diseases; Infections
|
Disease or Syndrome
|
430
|
80
|
0.010 |
None |
1.000 |
1 |
|
2016 |
2016 |