Retinitis punctata albescens (disorder)
|
disease |
Eye Diseases
|
Disease or Syndrome
|
10
|
10
|
0.700 |
None |
1.000 |
12 |
5
|
1999 |
2017 |
Autosomal recessive retinitis pigmentosa
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Congenital Abnormality
|
82
|
31
|
0.070 |
None |
1.000 |
7 |
2
|
1997 |
2013 |
Fundus Albipunctatus
|
disease |
Eye Diseases
|
Congenital Abnormality
|
9
|
21
|
0.730 |
None |
1.000 |
7 |
2
|
1997 |
2015 |
Retinal Diseases
|
group |
Eye Diseases
|
Disease or Syndrome
|
714
|
56
|
0.030 |
None |
1.000 |
3 |
|
2004 |
2015 |
Pigmentary retinal dystrophy
|
disease |
Eye Diseases
|
Disease or Syndrome
|
9
|
4
|
0.030 |
None |
1.000 |
3 |
1
|
2001 |
2015 |
Retinitis
|
disease |
Eye Diseases
|
Disease or Syndrome
|
20
|
1
|
0.020 |
None |
1.000 |
2 |
|
2004 |
2005 |
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 |
< 0.001 |
1 |
|
1990 |
1990 |
Degenerative polyarthritis
|
disease |
Musculoskeletal Diseases
|
Disease or Syndrome
|
1827
|
247
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Adenomatous Polyposis Coli
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
609
|
237
|
0.010 |
None |
1.000 |
1 |
|
2012 |
2012 |
Cone Dystrophy
|
disease |
Eye Diseases
|
Disease or Syndrome
|
48
|
31
|
0.010 |
None |
1.000 |
1 |
|
2012 |
2012 |
Uveitis
|
disease |
Eye Diseases
|
Disease or Syndrome
|
247
|
43
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
74
|
68
|
0.010 |
None |
1.000 |
1 |
|
2012 |
2012 |
Usher syndrome, type 1A
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases
|
Disease or Syndrome
|
14
|
2
|
0.010 |
None |
< 0.001 |
1 |
|
1990 |
1990 |
Neoplasms
|
group |
Neoplasms
|
Neoplastic Process
|
10161
|
1644
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Carcinogenesis
|
phenotype |
Pathological Conditions, Signs and Symptoms; Neoplasms
|
Neoplastic Process
|
6243
|
355
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Eye Diseases, Hereditary
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
9
|
|
0.300 |
None |
1.000 |
1 |
|
2007 |
2007 |
Age related macular degeneration
|
disease |
Eye Diseases
|
Disease or Syndrome
|
685
|
663
|
0.400 |
None |
1.000 |
1 |
|
2019 |
2019 |
Retinal Dystrophies
|
group |
Eye Diseases
|
Disease or Syndrome
|
219
|
227
|
0.110 |
None |
1.000 |
1 |
|
2006 |
2006 |
Schizophrenia
|
disease |
Mental Disorders
|
Mental or Behavioral Dysfunction
|
2872
|
2897
|
0.010 |
None |
1.000 |
1 |
|
2009 |
2009 |
Anteverted nostril
|
phenotype |
|
Finding
|
407
|
35
|
0.100 |
None |
|
0 |
|
|
|
Photophobia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Sign or Symptom
|
227
|
7
|
0.100 |
None |
|
0 |
|
|
|
Progressive visual loss
|
phenotype |
|
Finding
|
77
|
11
|
0.100 |
None |
|
0 |
|
|
|
Atrophoderma maculatum
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
39
|
2
|
0.100 |
None |
|
0 |
|
|
|
Nasal bridge wide
|
phenotype |
|
Finding
|
429
|
29
|
0.100 |
None |
|
0 |
|
|
|
Retinal pigment epithelial mottling
|
phenotype |
|
Finding
|
16
|
2
|
0.100 |
None |
|
0 |
|
|
|