RETINITIS PIGMENTOSA 3
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
8
|
31
|
0.970 |
None |
1.000 |
27 |
30
|
1996 |
2014 |
Retinitis Pigmentosa
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
546
|
541
|
0.800 |
strong |
1.000 |
79 |
23
|
1995 |
2019 |
CONE-ROD DYSTROPHY, X-LINKED, 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
1
|
6
|
0.800 |
None |
1.000 |
3 |
6
|
1998 |
2003 |
Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Infections; Eye Diseases; Respiratory Tract Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases
|
Disease or Syndrome
|
1
|
2
|
0.700 |
None |
1.000 |
4 |
2
|
1998 |
2006 |
MACULAR DEGENERATION, X-LINKED ATROPHIC
|
disease |
|
Disease or Syndrome
|
1
|
|
0.500 |
None |
1.000 |
1 |
|
1998 |
1998 |
Retinal Dystrophies
|
group |
Eye Diseases
|
Disease or Syndrome
|
219
|
227
|
0.460 |
None |
1.000 |
8 |
3
|
2002 |
2019 |
Age related macular degeneration
|
disease |
Eye Diseases
|
Disease or Syndrome
|
685
|
663
|
0.430 |
None |
1.000 |
3 |
|
2002 |
2019 |
X-linked retinitis pigmentosa
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Congenital Abnormality
|
29
|
7
|
0.400 |
strong |
0.989 |
94 |
3
|
1995 |
2020 |
Cone-Rod Dystrophy 2
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
254
|
51
|
0.390 |
None |
1.000 |
10 |
|
2002 |
2019 |
Primary Ciliary Dyskinesia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases
|
Disease or Syndrome
|
160
|
10
|
0.340 |
None |
1.000 |
4 |
|
2005 |
2018 |
Ciliopathies
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
241
|
7
|
0.330 |
None |
1.000 |
3 |
|
2008 |
2018 |
Retinal Degeneration
|
phenotype |
Eye Diseases
|
Pathologic Function
|
125
|
2
|
0.310 |
None |
1.000 |
2 |
|
2002 |
2009 |
Kartagener Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
67
|
3
|
0.310 |
None |
1.000 |
1 |
|
2018 |
2018 |
Disorder of eye
|
group |
Eye Diseases
|
Disease or Syndrome
|
400
|
14
|
0.310 |
None |
1.000 |
1 |
|
2009 |
2009 |
Respiratory Tract Infections
|
group |
Infections; Respiratory Tract Diseases
|
Disease or Syndrome
|
187
|
10
|
0.300 |
None |
1.000 |
1 |
|
2003 |
2003 |
Upper Respiratory Infections
|
group |
Infections; Respiratory Tract Diseases
|
Disease or Syndrome
|
64
|
6
|
0.300 |
None |
1.000 |
1 |
|
2003 |
2003 |
hearing impairment
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
|
Disease or Syndrome
|
740
|
337
|
0.300 |
None |
1.000 |
1 |
|
2003 |
2003 |
Achromatopsia
|
disease |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
26
|
63
|
0.300 |
None |
|
0 |
|
|
|
Polynesian Bronchiectasis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
35
|
|
0.300 |
None |
|
0 |
|
|
|
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
43
|
67
|
0.300 |
None |
|
0 |
|
|
|
CONE DYSTROPHY, X-LINKED, 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
4
|
|
0.210 |
None |
1.000 |
3 |
|
2000 |
2003 |
Cone-Rod Dystrophies
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
86
|
53
|
0.200 |
None |
1.000 |
10 |
|
1995 |
2018 |
Hereditary retinal dystrophy
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
42
|
1
|
0.200 |
None |
1.000 |
4 |
|
2000 |
2012 |
Blindness
|
phenotype |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
393
|
34
|
0.180 |
None |
1.000 |
8 |
|
2002 |
2019 |
Cone Dystrophy
|
disease |
Eye Diseases
|
Disease or Syndrome
|
48
|
31
|
0.160 |
None |
1.000 |
6 |
1
|
1997 |
2016 |