| Diseases |
Alias |
|
| Retinitis Pigmentosa 3 |
|
RP3
|
Retinitis Pigmentosa 15
|
|
Rp15
|
Choroidoretinal Degeneration With Retinal Reflex In Heterozygous Women
|
|
Cone-Rod Degeneration, X-Linked
|
Retinitis Pigmentosa Type 15
|
|
X-Linked Cone-Rod Degeneration
|
X-Linked Retinitis Pigmentosa 3
|
|
Xlrp3
|
Xlrp-3
|
|
Retinitis Pigmentosa-3
|
Retinitis Pigmentosa, Type 3
|
|
|
| Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness |
|
Retinitis Pigmentosa And Sinorespiratory Infections With Or Without Deafness
|
RPDSI
|
|
X-Linked Retinitis Pigmentosa With Deafness And Sinorespiratory Infections
|
Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Deafness
|
|
Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With/Without Deafness
|
|
|
| Cone-Rod Dystrophy, X-Linked, 1 |
|
CORDX1
|
X-Linked Cone-Rod Dystrophy 1
|
|
Cod1
|
Cone Dystrophy X-Linked 1
|
|
X-Linked Cone Dystrophy 1
|
Cone-Rod Dystrophy X-Linked 1
|
|
Cone-Rod Dystrophy, X-Linked 1
|
Dystrophy, Cone-Rod, X-Linked, Type 1
|
|
Cone Dystrophy, X-Linked, 1
|
|
|
| Macular Degeneration, X-Linked Atrophic |
|
X-Linked Atrophic Macular Degeneration
|
Macular Degeneration, X-Linked, Atrophic
|
|
MDXLA
|
Degeneration, Macular, X-Linked Atrophic
|
|
|
| Cone-Rod Dystrophy 2 |
|
Cone-Rod Dystrophy
|
CORD2
|
|
Cone-Rod Retinal Dystrophy
|
Rcrd2
|
|
Cone-Rod Retinal Dystrophy 2
|
Crd2
|
|
Cord
|
Crd
|
|
Retinal Cone-Rod Dystrophy
|
Cone-Rod Retinal Dystrophy-2
|
|
Retinal Cone-Rod Dystrophy 2
|
Tapetoretinal Degeneration
|
|
Cone-Rod Degeneration
|
Cone Rod Dystrophy
|
|
Dystrophy, Cone-Rod
|
Dystrophy, Cone-Rod, Type 2
|
|
Retinitis Pigmentosa
|
Retinitis Pigmentosa 2
|
|
Progressive Cone-Rod Dystrophy
|
|
|
| X-Linked Retinitis Pigmentosa And Sinorespiratory Infections |
|
Primary Ciliary Dyskinesia-Retinitis Pigmentosa Syndrome
|
|
|
| Retinitis Pigmentosa |
|
RP
|
Rod-Cone Dystrophy
|
|
Autosomal Recessive Retinitis Pigmentosa
|
Non-Syndromic Retinitis Pigmentosa
|
|
Pericentral Pigmentary Retinopathy
|
Pigmentary Retinopathy
|
|
Tapetoretinal Degeneration
|
Rcd
|
|
Retinitis Pigmentosa Autosomal Recessive
|
ARRP
|
|
Retinitis Pigmentosa, Autosomal Recessive
|
Retinitis Pigmentosa 1
|
|
|
| Cone Dystrophy |
|
Retinal Cone Dystrophy
|
Dystrophy, Cone
|
|
Cone Dystrophy 3
|
|
|
| Primary Ciliary Dyskinesia |
|
Immotile Cilia Syndrome
|
Kartagener Syndrome
|
|
Dextrocardia Bronchiectasis And Sinusitis
|
Pcd
|
|
Ciliary Motility Disorders
|
Ciliary Motility Disorder
|
|
Immotile Ciliary Syndrome
|
Ciliary Dyskinesia Primary
|
|
Ics
|
Polynesian Bronchiectasis
|
|
Dextrocardia-Bronchiectasis-Sinusitis Syndrome
|
Immotile Cilia Syndrome, Kartagener Type
|
|
Primary Ciliary Dyskinesia And Situs Inversus
|
Primary Ciliary Dyskinesia, Kartagener Type
|
|
Siewert Syndrome
|
Dyskinesia, Ciliary, Primary
|
|
|
| Fundus Dystrophy |
|
Retinal Dystrophy
|
Retinal Dystrophies
|
|
Dystrophy, Retinal
|
|
|
| Retinitis |
|
|
| Retinitis Pigmentosa 6 |
|
RP6
|
Retinitis Pigmentosa, X-Linked Recessive, 6
|
|
Retinitis Pigmentosa-6, X-Linked Recessive
|
|
|
| Achromatopsia |
|
Achm
|
Rod Monochromatism
|
|
Total Color Blindness
|
Rod Monochromacy
|
|
Monochromatism
|
Achromatism
|
|
Complete Or Incomplete Color Blindness
|
Pingelapese Blindness
|
|
Achromatopsia 1
|
Achromatopsia 2
|
|
Achromatopsia 3
|
|
|
| Congenital Stationary Night Blindness |
|
Night Blindness, Congenital Stationary
|
Congenital Essential Nyctalopia
|
|
Oguchi Disease
|
Blindness, Night, Stationary, Congenital
|
|
|
| Retinoschisis 1, X-Linked, Juvenile |
|
Retinoschisis
|
X-Linked Retinoschisis
|
|
X-Linked Juvenile Retinoschisis
|
RS1
|
|
XLRS1
|
X-Linked Juvenile Retinoschisis 1
|
|
Xlrs
|
Retinoschisis, X-Linked
|
|
Rs
|
Congenital X-Linked Retinoschisis
|
|
Degenerative Retinoschisis
|
Juvenile Retinoschisis
|
|
Xjr
|
Retinoschisis Juvenile X-Linked 1
|
|
Retinoschisis, Juvenile, X-Linked
|
Retinoschisis, Degenerative
|
|
|
| Retinitis Pigmentosa 2 |
|
RP2
|
X-Linked Retinitis Pigmentosa 2
|
|
Xlrp2
|
Xlrp-2
|
|
Retinitis Pigmentosa-2
|
Retinitis Pigmentosa, Type 2
|
|
|
| Myopia |
|
Near-Sightedness
|
Short-Sightedness
|
|
Nearsightedness
|
Nearsighted
|
|
Near Vision
|
Close Sighted
|
|
Myopic
|
Short-Sighted
|
|
Near Sighted
|
|
|
| Retinal Degeneration |
|
|
| Retinitis Pigmentosa 19 |
|
RP19
|
Retinitis Pigmentosa-19
|
|
Retinitis Pigmentosa, Type 19
|
|
|
| Retinitis Pigmentosa 23 |
|
RP23
|
Retinitis Pigmentosa-23
|
|
Retinitis Pigmentosa, Type 23
|
Rp23 Gene
|
|
|
| Retinitis Pigmentosa 24 |
|
RP24
|
Retinitis Pigmentosa-24
|
|
|
| Retinitis Pigmentosa 27 |
|
RP27
|
Retinal Degeneration, Autosomal Recessive, Clumped Pigment Type
|
|
Retinal Degeneration Autosomal Recessive Clumped Pigment Type
|
RDCP
|
|
Clumped Pigmentary Retinal Degeneration
|
Retinitis Pigmentosa, Type 27
|
|
|
| Stargardt Disease |
|
Stargardt Disease 1
|
Stargardt Macular Dystrophy
|
|
Stargardt Disease-1
|
Juvenile Onset Macular Degeneration
|
|
Stargardt Macular Degeneration
|
Juvenile Macular Degeneration
|
|
Macular Dystrophy With Flecks, Type 1
|
Stgd
|
|
Fundus Flavimaculatus
|
Stargardt 1
|
|
Stargardts Disease
|
|
|
| Retinitis Pigmentosa 40 |
|
RP40
|
Retinitis Pigmentosa-40
|
|
Retinitis Pigmentosa, Type 40
|
|
|
| Retinitis Pigmentosa 67 |
|
RP67
|
Retinitis Pigmentosa, Type 67
|
|
|
| Night Blindness |
|
|
| Cone-Rod Dystrophy 13 |
|
CORD13
|
Dystrophy, Cone-Rod, Type 13
|
|
|
| Choroid Disease |
|
Choroid Diseases
|
Abnormality Of The Choroid
|
|
|
| Retinitis Pigmentosa 35 |
|
RP35
|
Retinitis Pigmentosa-35
|
|
Retinitis Pigmentosa, Type 35
|
|
|
| Leber Congenital Amaurosis 10 |
|
LCA10
|
Leber Congenital Amaurosis, Type 10
|
|
|
| Eye Degenerative Disease |
|
|
| Scotoma |
|
Enlarged Blind Spot
|
Scotoma Of Blind Spot Area
|
|
Blind Spot Area Scotoma
|
Enlarged Angioscotoma
|
|
Enlarged Paracaecal Scotoma
|
Generalized Visual Field Contraction Or Constriction
|
|
Sector Or Arcuate Visual Field Defects
|
|
|
| Cone-Rod Dystrophy 1 |
|
CORD1
|
Crd1
|
|
Cone-Rod Retinal Dystrophy-1
|
Retinitis Pigmentosa 1
|
|
|
| Bietti Crystalline Corneoretinal Dystrophy |
|
BCD
|
Bietti Crystalline Dystrophy
|
|
Bietti Tapetoretinal Degeneration With Marginal Corneal Dystrophy
|
Bietti Crystalline Retinopathy
|
|
Bietti'S Crystalline Dystrophy
|
Crystalline Retinopathy
|
|
Dystrophy, Corneoretinal, Crystalline, Bietti
|
|
|
| Retinitis Pigmentosa 85 |
|
RP85
|
Retinitis Pigmentosa, Type 85
|
|
|
| Retinitis Pigmentosa 74 |
|
RP74
|
Retinitis Pigmentosa, Type 74
|
|
|
| Retinitis Pigmentosa 39 |
|
RP39
|
Retinitis Pigmentosa, Type 39
|
|
|
| Joubert Syndrome 7 |
|
JBTS7
|
Cerebello-Oculo-Renal Syndrome 3
|
|
Cors3
|
Joubert Syndrome, Type 7
|
|
|
| Usher Syndrome |
|
Deafness-Retinitis Pigmentosa Syndrome
|
Dystrophia Retinae Pigmentosa-Dysostosis Syndrome
|
|
Graefe-Usher Syndrome
|
Hallgren Syndrome
|
|
Usher'S Syndrome
|
Retinitis Pigmentosa-Deafness Syndrome
|
|
Retinitis Pigmentosa-Hearing Loss Syndrome
|
Ush
|
|
Usher Syndromes
|
|
|
| Retinitis Pigmentosa 75 |
|
RP75
|
Retinitis Pigmentosa, Type 75
|
|
|
| Retinitis Pigmentosa 25 |
|
RP25
|
Retinitis Pigmentosa-25
|
|
Retinitis Pigmentosa, Type 25
|
|
|
| Progressive Cone Dystrophy |
|
Cone Dystrophy
|
Cone Dystrophy Progressive
|
|
|
| Cone-Rod Dystrophy, X-Linked, 3 |
|
CORDX3
|
X-Linked Cone-Rod Dystrophy 3
|
|
Cone-Rod Dystrophy X-Linked 3
|
Cone-Rod Dystrophy, X-Linked 3
|
|
Dystrophy, Cone-Rod, X-Linked, Type 3
|
|
|
| Retinitis Pigmentosa 12 |
|
RP12
|
Retinitis Pigmentosa With Or Without Paraarteriolar Preservation Of Retinal Pigment Epithelium
|
|
Rp With Or Without Preserved Paraarteriole Retinal Pigment Epithelium
|
Rp With Or Without Pprpe
|
|
Retinitis Pigmentosa-12
|
|
|
| Retinitis Pigmentosa 17 |
|
RP17
|
Retinitis Pigmentosa-17
|
|
Retinitis Pigmentosa, Type 17
|
|
|
| Nephronophthisis 12 |
|
NPHP12
|
Joubert Syndrome 11
|
|
JBTS11
|
Nephronophthisis, Type 12
|
|
|
| Leber Plus Disease |
|
Leber Congenital Amaurosis
|
Lca
|
|
Leber'S Amaurosis
|
Leber'S Disease
|
|
Amaurosis Congenita Of Leber
|
Amaurosis Congenita Of Leber, Type 1
|
|
Lhon Plus Disease
|
Congenital Absence Of The Rods And Cones
|
|
Congenital Retinal Blindness
|
Crb
|
|
Congenital Amaurosis Of Retinal Origin
|
Leber'S Congenital Amaurosis
|
|
Leber Congenital Amaurosis 1
|
Leber'S Congenital Tapetoretinal Degeneration
|
|
Leber'S Congenital Tapetoretinal Dysplasia
|
Lca1
|
|
Leber Congenital Amaurosis Type 1
|
Retinal Blindness, Congenital
|
|
Amaurosis, Leber Congenital
|
Dysgenesis Neuroepithelialis Retinae
|
|
Hereditary Epithelial Dysplasia Of Retina
|
Hereditary Retinal Aplasia
|
|
Heredoretinopathia Congenitalis
|
Leber Abiotrophy
|
|
Leber Congenital Tapetoretinal Degeneration
|
Lebers Congenital Amaurosis
|
|
Optic Atrophy, Hereditary, Leber
|
|
|
| Enhanced S-Cone Syndrome |
|
Goldmann-Favre Syndrome
|
ESCS
|
|
Favre Hyaloideoretinal Degeneration
|
Retinoschisis With Early Hemeralopia
|
|
Retinoschisis With Early Nyctalopia
|
Enhanced S Cone Syndrome
|
|
S-Cone Syndrome, Enhanced
|
|
|
| Retinitis Pigmentosa 38 |
|
RP38
|
Rod-Cone Dystrophy, Childhood-Onset
|
|
Retinitis Pigmentosa, Type 38
|
|
|
| Macular Dystrophy, Dominant Cystoid |
|
Cystoid Macular Edema
|
DCMD
|
|
Cystoid Macular Dystrophy
|
Macular Edema, Cystoid
|
|
Autosomal Dominant Cystoid Macular Edema
|
Cymd
|
|
Mddc
|
Familial Macular Edema
|
|
Macular Edema
|
Macular Retinal Edema
|
|
|
| Gyrate Atrophy Of Choroid And Retina |
|
Gyrate Atrophy
|
Ornithine Aminotransferase Deficiency
|
|
HOGA
|
Hyperornithinemia With Gyrate Atrophy Of Choroid And Retina
|
|
Oat Deficiency
|
Okt Deficiency
|
|
Hyperornithinemia
|
Ornithine Keto Acid Aminotransferase Deficiency
|
|
Ornithine-Delta-Aminotransferase Deficiency
|
Gyrate Atrophy Of The Choroid And Retina
|
|
GACR
|
Gyrate Atrophy Of Choroid And Retina With Or Without Ornithinemia
|
|
Gyrate Atrophy Of The Retina
|
Ornithinemia With Gyrate Atrophy
|
|
Ornithinemia
|
Fuchs Atrophia Gyrata Chorioideae Et Retinae
|
|
Hyperornithinemia-Gyrate Atrophy Of Choroid And Retina Syndrome
|
Gyrate Atrophy Of The Choroid And/Or Retina
|
|
Girate Atrophy Of The Retina
|
Ornithine Ketoacid Aminotransferase Deficiency
|
|
Atrophy, Gyrate, Of Choroid And Retina
|
|
|
| Nephronophthisis |
|
Medullary Cystic Disease
|
Medullary Cystic Kidney
|
|
Nph
|
Nphp
|
|
Kidney Disease, Cystic, Medullary
|
|
|
| Senior-Loken Syndrome 1 |
|
Senior-Loken Syndrome
|
Renal Dysplasia And Retinal Aplasia
|
|
Renal-Retinal Syndrome
|
Loken-Senior Syndrome
|
|
Juvenile Nephronophthisis With Leber Amaurosis
|
SLSN1
|
|
Senior-Loken Syndrome-1
|
Loken Senior Syndrome
|
|
Senior Loken Syndrome
|
Renal Dysplasia Retinal Aplasia
|
|
Nephronophthisis With Retinal Dystrophy
|
Renal Dysplasia-Retinal Aplasia Syndrome
|
|
Slsn
|
|
|
| Occult Macular Dystrophy |
|
OCMD
|
Omd
|
|
Dystrophy, Macular, Occult
|
|
|
| Color Blindness |
|
Color Vision Defect
|
Blindness Color
|
|
Colour Blindness
|
Colour Vision Deficiency
|
|
Color Vision Deficiency
|
Color Vision Defects
|
|
Defective Color Vision
|
Vision Defect, Color
|
|
Color-Vision Disease
|
Dyschromatopsia
|
|
|
| Macular Degeneration, Age-Related, 1 |
|
Macular Degeneration
|
Age-Related Macular Degeneration
|
|
Macular Degeneration, Age-Related
|
Age Related Macular Degeneration
|
|
Age Related Macular Degeneration 1
|
ARMD1
|
|
Senile Macular Degeneration
|
Maculopathy, Age-Related, 1
|
|
Macular Degeneration, Age-Related, Reduced Risk Of
|
Age Related Maculopathy 1
|
|
Age Related Maculopathies
|
Age Related Maculopathy
|
|
Senile Macular Retinal Degeneration
|
Macular Degeneration Of Retina
|
|
Age-Related Maculopathy
|
Amd
|
|
Armd
|
Age-Related Maculopathy, Susceptibility To
|
|
Maculopathy Age-Related
|
Macular Degeneration, Age-Related, 1, Susceptibility To
|
|
Maculopathy, Age-Related
|
Macular Degeneration, Age-Related, Type 1
|
|
Macular Degeneration, Age-Related, 2
|
|
|
| Blue Cone Monochromacy |
|
Blue Cone Monochromatism
|
BCM
|
|
Cbbm
|
Color Blindness Blue Mono Cone Monochromatic Type
|
|
Cone Dystrophy 5, X-Linked
|
Colorblindness, Blue-Mono-Cone-Monochromatic Type
|
|
Achromatopsia Incomplete X-Linked
|
Incomplete Achromatopsia X-Linked
|
|
X-Chromosome-Linked Achromatopsia
|
X-Linked Achromatopsia Incomplete
|
|
Atypical X-Linked Achromatopsia
|
Color Blindness, Blue Monocone Monochromatic Type
|
|
S Cone Monochromacy
|
S Cone Monochromatism
|
|
X-Linked Incomplete Achromatopsia
|
Colorblindness Blue-Mono-Cone-Monochromatic Type
|
|
Cone Dystrophy 5
|
COD5
|
|
Cone Dystrophy 5 X-Linked
|
Monochromacy, Blue Cone
|
|
Cone Monochromatism
|
Achromatopsia Incomplete, X-Linked
|
|
|
| Ciliary Dyskinesia, Primary, 4 |
|
Primary Ciliary Dyskinesia 4
|
CILD4
|
|
Ciliary Dyskinesia, Primary, 4, With Or Without Situs Inversus
|
Primary Ciliary Dyskinesia 4 With Or Without Situs Inversus
|
|
Primary Ciliary Dyskinesia, 4
|
|
|
| Ciliary Dyskinesia, Primary, 8 |
|
Primary Ciliary Dyskinesia 8
|
CILD8
|
|
Ciliary Dyskinesia, Primary, 8, With Or Without Situs Inversus
|
Primary Ciliary Dyskinesia 8 With Or Without Situs Inversus
|
|
|
| Choroideremia |
|
CHM
|
Tcd
|
|
Progressive Tapetochoroidal Dystrophy
|
Choroidal Sclerosis
|
|
Tapetochoroidal Dystrophy, Progressive
|
Progressive Choroidal Atrophy
|
|
Tapetochoroidal Dystrophy
|
|
|
| Retinitis Pigmentosa 84 |
|
RP84
|
Retinitis Pigmentosa, Type 84
|
|
|
| Joubert Syndrome 1 |
|
Joubert Syndrome
|
Jbts
|
|
Cerebellooculorenal Syndrome 1
|
JBTS1
|
|
Joubert-Boltshauser Syndrome
|
Cerebelloparenchymal Disorder Iv
|
|
Cpd4
|
Cors1
|
|
Joubert Syndrome And Related Disorders
|
Jsrd
|
|
Familial Aplasia Of The Vermis
|
Joubert Syndrome Related Disorders
|
|
Js
|
Cerebellar Vermis Agenesis
|
|
Cerebelloparenchymal Disorder 4
|
Agenesis Of Cerebellar Vermis
|
|
Cerebello-Oculo-Renal Syndrome
|
Cors
|
|
Joubert-Bolthauser Syndrome
|
Cpd Iv
|
|
Classic Joubert Syndrome
|
Joubert Syndrome Type A
|
|
Pure Joubert Syndrome
|
Cerebello-Oculo-Renal Syndrome 1
|
|
Joubert Syndrome-1
|
Joubert Syndrome, Type 1
|
|
Joubert'S Syndrome
|
|
|
| Retinitis Pigmentosa 30 |
|
RP30
|
Retinitis Pigmentosa-30
|
|
Retinitis Pigmentosa, Type 30
|
|
|
| Cone-Rod Dystrophy 3 |
|
CORD3
|
Dystrophy, Cone Rod, Type 3
|
|
|
| Optic Disk Drusen |
|
Optic Disc Drusen
|
Drusen Of Optic Disc
|
|
Optic Nerve Head Drusen
|
Drusen Optic Disc
|
|
|
| Late-Onset Retinal Degeneration |
|
LORD
|
Retinal Degeneration, Late-Onset, Autosomal Dominant
|
|
Autosomal Dominant Late-Onset Retinal Degeneration
|
Pigmentary Retinopathy
|
|
Retinal Degeneration, Late-Onset
|
Retinitis Pigmentosa
|
|
|
| Vitelliform Macular Dystrophy |
|
Best Disease
|
Juvenile-Onset Vitelliform Macular Dystrophy
|
|
Macular Dystrophy, Vitelliform
|
Best Macular Dystrophy
|
|
Vitelliform Dystrophy
|
|
|
| Leber Congenital Amaurosis 2 |
|
LCA2
|
Amaurosis Congenita Of Leber Ii
|
|
Amaurosis Congenita Of Leber, Type 2
|
Leber Congenital Amaurosis Type Ii
|
|
Leber Congenital Amaurosis, Type 2
|
Leber Congenital Amaurosis, Type Ii
|
|
|
| Retinitis Pigmentosa 26 |
|
RP26
|
Retinitis Pigmentosa-26
|
|
Retinitis Pigmentosa, Type 26
|
|
|
| Peripheral Retinal Degeneration |
|
Peripheral Degeneration Of Retina
|
Degeneration Of Retina Nos
|
|
Reticular Retinal Degeneration
|
Retinal Degeneration
|
|
|
| Immunodeficiency 25 |
|
Immunodeficiency Due To Defect In Cd3-Zeta
|
IMD25
|
|
Immunodeficiency, Type 25
|
|
|
| Red-Green Color Blindness |
|
Deutan Defect
|
Deuteranopia
|
|
Reduced Red-Green Discrimination
|
Color Blindness, Red-Green
|
|
Colorblindness, Partial, Deutan Series
|
|
|
| Usher Syndrome Type 2 |
|
Ush2
|
Usher Syndrome Type Ii
|
|
|
| Refractive Error |
|
|
| Fundus Albipunctatus |
|
Retinitis Punctata Albescens
|
Pigmentary Retinal Dystrophy
|
|
RPA
|
Albipunctate Retinal Dystrophy
|
|
Lauber'S Disease
|
FALBI
|
|
Fa
|
|
|
| Nephronophthisis 19 |
|
NPHP19
|
Nephronophthisis, Type 19
|
|
|
| Bestrophinopathy, Autosomal Recessive |
|
Bestrophinopathy
|
Autosomal Recessive Bestrophinopathy
|
|
ARB
|
Bestrophinopathies
|
|
Retinopathy, Burgess-Black Type
|
Retinopathy Burgess-Black Type
|
|
|
| Retinitis Pigmentosa 31 |
|
RP31
|
Retinitis Pigmentosa-31
|
|
Retinitis Pigmentosa, Type 31
|
|
|
| Ciliary Dyskinesia, Primary, 43 |
|
CILD43
|
Primary Ciliary Dyskinesia 43
|
|
Ciliary Dyskinesia, Primary, 43, With Or Without Situs Inversus
|
Primary Ciliary Dyskinesia 43 With Or Without Situs Inversus
|
|
Ciliary Dyskinesia, Primary, 43 With Or Without Situs Inversus
|
|
|
| Retinitis Pigmentosa 54 |
|
RP54
|
Retinitis Pigmentosa, Type 54
|
|
|
| Exudative Vitreoretinopathy |
|
Familial Exudative Vitreoretinopathy
|
Fevr
|
|
Criswick-Schepens Syndrome
|
Exudative Vitreoretinopathy, Familial
|
|
Vitreoretinopathy, Exudative )
|
Exudative Vitreoretinopathy 1
|
|
|
| Usher Syndrome, Type Iia |
|
Usher Syndrome Type 2a
|
USH2A
|
|
Usher Syndrome, Type 2a
|
Usher Syndrome Type Iia
|
|
Retinal Disease In Usher Syndrome Type Iia, Modifier Of
|
Us2
|
|
Ush2
|
Usher Syndrome 2a
|
|
Usher'S Syndrome Type 2a
|
Ushiia
|
|
|
| Vitreous Syneresis |
|
|
| Retinal Disease |
|
Retinal Diseases
|
Retinal Disorder
|
|
Retinal Disorders
|
|
|
| Ciliary Dyskinesia, Primary, 1 |
|
CILD1
|
Pcd
|
|
Primary Ciliary Dyskinesia 1
|
Kartagener Syndrome
|
|
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
|
Immotile Cilia Syndrome
|
|
Ics
|
Polynesian Bronchiectasis
|
|
Primary Ciliary Dyskinesia 1 With Or Without Situs Inversus
|
Ics1
|
|
Immotile Cilia Syndrome 1
|
Primary Ciliary Dyskinesia
|
|
KTGS
|
Dextrocardia-Bronchiectasis-Sinusitis Syndrome
|
|
Immotile Cilia Syndrome Kartagener Type
|
Primary Ciliary Dyskinesia Kartagener Type
|
|
Siewert Syndrome
|
Immotile Cilia
|
|
Dyskinesia, Ciliary, Primary, Type 1
|
Ciliary Motility Disorders
|
|
|
| Choroidal Dystrophy, Central Areolar, 1 |
|
Choroidal Sclerosis
|
Choroidal Dystrophy
|
|
Choroidal Dystrophy, Central Areolar
|
Cacd
|
|
Central Areolar Choroidal Dystrophy
|
CACD1
|
|
Choroidal Dystrophy, Central Areolar 1
|
Choroidal Dystrophy Central Areolar
|
|
Central Areolar Choroidal Sclerosis
|
Choroidal Degenerations
|
|
Areolar Atrophy Of The Macula
|
Partial Central Choroid Dystrophy
|
|
Degenerative Choroidopathy
|
Chorioretinal Degeneration
|
|
Hereditary Chorioretinal Degeneration
|
Hereditary Degeneration Of Choroid
|
|
Hereditary Choroidal Dystrophies
|
Generalised Choroidal Dystrophy
|
|
Hereditary Choroidopathy
|
|
|
| Muscular Dystrophy, Duchenne Type |
|
Duchenne Muscular Dystrophy
|
DMD
|
|
Muscular Dystrophy, Duchenne
|
Muscular Dystrophy, Pseudohypertrophic Progressive, Duchenne Type
|
|
Severe Dystrophinopathy, Duchenne Type
|
Muscular Dystrophy Duchenne
|
|
Dystrophy, Muscular, Duchenne Type
|
Benign Duchenne Muscular Dystrophy
|
|
Duchenne Motor Neuron Disease
|
Duchenne Type Dystrophy
|
|
Duchenne-Griesinger Disease
|
|
|
| Degeneration Of Macula And Posterior Pole |
|
Degeneration Of Macula And Posterior Pole Of Retina
|
Degeneration Of Macula Or Posterior Pole
|
|
Macular Degeneration Nos
|
Degenerative Disorder Of Macula
|
|
Drusen Macular Degeneration
|
Posterior Pole Macular Degeneration Of Eye
|
|
Macular Eye Degeneration
|
Macular Degeneration Of Retina, Unspecified
|
|
Pseudohole Degeneration Of Macula Of Retina
|
|
|
| Cone-Rod Dystrophy 16 |
|
Retinitis Pigmentosa 64
|
Retinal Dystrophy With Early Macular Involvement
|
|
CORD16
|
RP64
|
|
|
| Achromatopsia 7 |
|
ACHM7
|
Achromatopsia, Type 7
|
|
|
| Sensory System Disease |
|
|
| Kartagener Syndrome |
|
|
| Usher Syndrome, Type I |
|
USH1
|
Usher Syndrome Type 1
|
|
Us1
|
Usher Syndrome, Type 1b
|
|
Usher Syndrome Type 1e
|
Retinitis Pigmentosa And Congenital Deafness
|
|
Usher Syndrome, Type Ie
|
USH1E
|
|
Usher Syndrome, Type 1e
|
Usher Syndrome, Type 1a
|
|
Usher Syndrome, Type Ib
|
Usher Syndrome Type 1b
|
|
Usher Syndrome Type Ie
|
Usher Syndrome Type I
|
|
Usher 1
|
Usher Syndrome, Type 1
|
|
Ush1a
|
Usher Syndrome, Type I, French Variety
|
|
Usher Syndrome, Type Ia
|
Usher Syndrome 1b
|
|
USH1B
|
Usher'S Syndrome Type 1b
|
|
Usher Syndrome Type Ib
|
Ushib
|
|
|
| Visceral Heterotaxy |
|
Situs Ambiguus
|
Heterotaxia
|
|
Heterotaxy Syndrome
|
Heterotaxy
|
|
Lateralization Defect
|
Situs Ambiguous
|
|
Left Isomerism
|
Htx
|
|
Ivemark Syndrome
|
Right Isomerism
|
|
Situs Ambiguus Viscerum
|
Incomplete Situs Inversus
|
|
Partial Situs Inversus
|
Heterotaxy, Visceral
|
|
Asplenia Syndrome
|
Bilateral Left-Sidedness
|
|
Polysplenia Syndrome
|
Moller Syndrome
|
|
|
| Cranioectodermal Dysplasia |
|
Sensenbrenner Syndrome
|
Levin Syndrome 1
|
|
Ced
|
Levin Syndrome
|
|
Dysplasia, Cranioectodermal
|
|
|
| Nanophthalmos |
|
|
| Stickler Syndrome |
|
Arthroophthalmopathy
|
Hereditary Arthro-Ophthalmo-Dystrophy
|
|
Hereditary Arthro-Ophthalmopathy
|
Stickler Dysplasia
|
|
Hereditary Progressive Arthroophthalmopathy
|
Stickler Syndrome, Type 1
|
|
|
| Situs Inversus |
|
Situs Inversus Viscerum
|
Laterality Sequence
|
|
Complete Transposition
|
Siv
|
|
|
| Meckel Syndrome, Type 1 |
|
Meckel-Gruber Syndrome
|
Meckel Syndrome
|
|
Dysencephalia Splanchnocystica
|
Meckel Syndrome 1
|
|
MKS1
|
Mks
|
|
Gruber Syndrome
|
Meckel-Gruber Syndrome, Type 1
|
|
Mes
|
Dysencephalia Splachnocystica
|
|
Meckel Gruber Syndrome
|
Meckel Syndrome Type 1
|
|
|
| Eye Disease |
|
Eye Diseases
|
Abnormality Of The Eye
|
|
Toxoplasma Oculopathy
|
|
|
| Leber Hereditary Optic Neuropathy, Modifier Of |
|
Leber Optic Atrophy
|
Leber Hereditary Optic Neuropathy
|
|
LHON
|
Leber'S Hereditary Optic Neuropathy
|
|
Leber Optic Atrophy, Susceptibility To
|
Leber'S Optic Atrophy
|
|
LOAM
|
Loas
|
|
Leber'S Disease
|
Leber'S Optic Neuropathy
|
|
Optic Atrophy, Hereditary, Leber
|
Lhon, Modifier Of
|
|
Optic Atrophy, Leber Type
|
Hereditary Optic Neuroretinopathy
|
|
Leber Hereditary Optic Atrophy
|
Loa
|
|
Optic Atrophy Leber Type
|
Leber Hereditary Optic Neuropathy, Modifier
|
|
Leber Hereditary Optic Neuropathy Susceptibility
|
Modifier Of Leber Hereditary Optic Neuropathy
|
|
Lebers Hereditary Optic Neuropathy
|
Leber Congenital Amaurosis
|
|
|
| Asphyxiating Thoracic Dystrophy |
|
Jeune Thoracic Dystrophy
|
Jeune Syndrome
|
|
Asphyxiating Thoracic Dysplasia
|
Short-Rib Thoracic Dysplasia With Or Without Polydactyly
|
|
Thoracic Pelvic Phalangeal Dystrophy
|
Asphyxiating Thoracic Chondrodystrophy
|
|
Atd
|
Chondroectodermal Dysplasia-Like Syndrome
|
|
Infantile Thoracic Dystrophy
|
Jeune Thoracic Dysplasia
|
|
Thoracic Asphyxiant Dystrophy
|
Thoracic-Pelvic-Phalangeal Dystrophy
|
|
Short-Rib Thoracic Dysplasia Without Polydactyly
|
Asphyxiating Thoracic Dystrophy Of The Newborn
|
|
Asphyxiating Thorax Dystrophy
|
|
|
| Bardet-Biedl Syndrome |
|
Bbs
|
Biedl-Bardet Syndrome
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
