Retinitis Pigmentosa 4
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
1
|
44
|
0.910 |
None |
1.000 |
35 |
44
|
1990 |
2018 |
Night Blindness, Congenital Stationary, Autosomal Dominant 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
1
|
5
|
0.900 |
limited |
1.000 |
11 |
5
|
1993 |
2011 |
Night blindness, congenital stationary
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Congenital Abnormality
|
32
|
52
|
0.800 |
strong |
1.000 |
14 |
3
|
1993 |
2016 |
Retinitis punctata albescens (disorder)
|
disease |
Eye Diseases
|
Disease or Syndrome
|
10
|
10
|
0.720 |
strong |
1.000 |
2 |
1
|
1996 |
2005 |
Fundus Albipunctatus
|
disease |
Eye Diseases
|
Congenital Abnormality
|
9
|
21
|
0.710 |
limited |
1.000 |
2 |
1
|
1987 |
1996 |
Retinitis Pigmentosa
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
546
|
541
|
0.700 |
strong |
0.989 |
186 |
38
|
1978 |
2020 |
Retinal Degeneration
|
phenotype |
Eye Diseases
|
Pathologic Function
|
125
|
2
|
0.300 |
None |
1.000 |
2 |
|
1996 |
2016 |
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
26
|
9
|
0.300 |
None |
1.000 |
1 |
|
1993 |
1993 |
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
12
|
8
|
0.300 |
None |
1.000 |
1 |
|
1993 |
1993 |
X-Linked Csnb
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
13
|
|
0.300 |
None |
1.000 |
1 |
|
1993 |
1993 |
Cone-rod synaptic disorder, congenital nonprogressive
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
14
|
4
|
0.300 |
None |
1.000 |
1 |
|
1993 |
1993 |
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
12
|
|
0.300 |
None |
1.000 |
1 |
|
1993 |
1993 |
Night blindness, congenital stationary, type 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
12
|
|
0.300 |
None |
1.000 |
1 |
|
1993 |
1993 |
Night Blindness, Congenital Stationary, Type 1A
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
13
|
19
|
0.300 |
None |
1.000 |
1 |
|
1993 |
1993 |
Disorder of eye
|
group |
Eye Diseases
|
Disease or Syndrome
|
400
|
14
|
0.300 |
limited |
|
0 |
|
|
|
Hereditary retinal dystrophy
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
42
|
1
|
0.200 |
None |
1.000 |
8 |
|
1997 |
2017 |
Nyctalopia
|
disease |
Eye Diseases
|
Disease or Syndrome
|
168
|
18
|
0.180 |
None |
1.000 |
8 |
4
|
1995 |
2019 |
Blindness
|
phenotype |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
393
|
34
|
0.170 |
None |
1.000 |
7 |
2
|
2002 |
2018 |
Photophobia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Sign or Symptom
|
227
|
7
|
0.160 |
None |
1.000 |
6 |
|
2000 |
2019 |
Rod-Cone Dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
194
|
33
|
0.110 |
None |
1.000 |
1 |
1
|
1998 |
1998 |
Macular Edema, Cystoid
|
disease |
Eye Diseases
|
Disease or Syndrome
|
49
|
3
|
0.110 |
None |
1.000 |
1 |
1
|
2012 |
2012 |
Intellectual Disability
|
group |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
|
Mental or Behavioral Dysfunction
|
2165
|
159
|
0.110 |
None |
1.000 |
1 |
|
2000 |
2000 |
Autosomal dominant retinitis pigmentosa
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Congenital Abnormality
|
85
|
65
|
0.100 |
None |
1.000 |
136 |
22
|
1988 |
2020 |
Photoreceptor degeneration
|
disease |
Eye Diseases
|
Disease or Syndrome
|
136
|
16
|
0.100 |
None |
1.000 |
17 |
4
|
1998 |
2019 |
Retinal Diseases
|
group |
Eye Diseases
|
Disease or Syndrome
|
714
|
56
|
0.100 |
None |
1.000 |
12 |
1
|
1999 |
2019 |