| 疾病名称 |
别名 |
|
| Retinitis Pigmentosa 4 |
|
RP4
|
Retinitis Pigmentosa 4, Autosomal Dominant Or Recessive
|
|
Retinitis Pigmentosa, Rhodopsin-Related
|
Retinitis Pigmentosa, Type 4
|
|
|
| Night Blindness, Congenital Stationary, Autosomal Dominant 1 |
|
Congenital Stationary Night Blindness Autosomal Dominant 1
|
CSNBAD1
|
|
Rhodopsin-Related Congenital Stationary Night Blindness
|
Night Blindness, Congenital Stationary, Rhodopsin-Related
|
|
Blindness, Night, Stationary, Congenital, Autosomal Dominant, Type 1
|
|
|
| Fundus Albipunctatus |
|
Retinitis Punctata Albescens
|
Pigmentary Retinal Dystrophy
|
|
RPA
|
Albipunctate Retinal Dystrophy
|
|
Lauber'S Disease
|
FALBI
|
|
Fa
|
|
|
| Night Blindness |
|
|
| Optic Disk Drusen |
|
Optic Disc Drusen
|
Drusen Of Optic Disc
|
|
Optic Nerve Head Drusen
|
Drusen Optic Disc
|
|
|
| Retinal Detachment |
|
Retinal Detachments
|
Rhegmatogenous Retinal Detachment
|
|
Ruptured Retina With Detachment
|
Retinal Hole With Detachment
|
|
|
| Coats Disease |
|
Exudative Retinopathy
|
Retinal Telangiectasis
|
|
Coats' Disease
|
Leber Miliary Aneurysm
|
|
Coats' Syndrome
|
Congenital Retinal Telangiectasia
|
|
|
| Neuropathy, Congenital Hypomyelinating, 2 |
|
Hypomyelinating Neuropathy, Congenital, 2
|
CHN2
|
|
|
| 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
|
|
|
| Cataract |
|
Cataracts
|
Cat - [Cataract]
|
|
Cataract Form
|
Lens Opacity
|
|
Lens Opacities
|
|
|
| Fundus Dystrophy |
|
Retinal Dystrophy
|
Retinal Dystrophies
|
|
Dystrophy, Retinal
|
|
|
| Congenital Stationary Night Blindness |
|
Night Blindness, Congenital Stationary
|
Congenital Essential Nyctalopia
|
|
Oguchi Disease
|
Blindness, Night, Stationary, Congenital
|
|
|
| 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
|
|
|
| Retinitis |
|
|
| Colorectal Cancer |
|
Colon Cancer
|
Colorectal Carcinoma
|
|
Colon Carcinoma
|
Colorectal Cancer, Susceptibility To
|
|
Carcinoma Of Colon
|
CRC
|
|
Colorectal Cancer With Chromosomal Instability, Somatic
|
Colon Cancer, Somatic
|
|
Colon Cancer, Susceptibility To
|
Colonic Neoplasms
|
|
Colorectal Neoplasms
|
Colorectal Cancer, Somatic
|
|
Colon Cancer, Advanced, Somatic
|
Colonic Carcinoma
|
|
Colorectal Carcinomas
|
Colon Cancers
|
|
Colorectal Cancers
|
Cancer, Colorectal, Somatic
|
|
Cancer, Colon
|
Cancer, Colorectal, Susceptibility To
|
|
Colorectal Neoplasm
|
Colonic Neoplasm
|
|
Malignant Tumor Of Colon
|
|
|
| Hereditary Retinal Dystrophy |
|
Hereditary Retinal Dystrophies
|
|
|
| Retinitis Pigmentosa 1 |
|
RP1
|
Retinitis Pigmentosa-1
|
|
Retinitis Pigmentosa, Type 1
|
|
|
| Xerophthalmia |
|
|
| Oguchi Disease |
|
Stationary Night Blindness, Oguchi Type
|
Congenital Stationary Night Blindness, Oguchi Type
|
|
Oguchi Syndrome
|
Oguchis Disease
|
|
|
| Keratomalacia |
|
Vitamin A Deficiency
|
Night Blindness
|
|
Retinol Deficiency
|
Xerotic Keratitis
|
|
VAD
|
Vitamin A
|
|
Hypovitaminosis A
|
Bitot Spots
|
|
Bitot Spots In The Young Child
|
Conjunctival Xerosis With Bitot'S Spots
|
|
Vitamin A Deficiency With Cornea Xerosis
|
Vitamin A Deficiency With Cornea Ulceration Or Xerosis
|
|
|
| Retinal Degeneration |
|
|
| Eye Degenerative Disease |
|
|
| Ocular Hypertension |
|
Hypertension, Ocular
|
Intraocular Pressure Increase
|
|
Oh - [Ocular Hypertension]
|
Oht - [Ocular Hypertension]
|
|
|
| Myopia |
|
Near-Sightedness
|
Short-Sightedness
|
|
Nearsightedness
|
Nearsighted
|
|
Near Vision
|
Close Sighted
|
|
Myopic
|
Short-Sighted
|
|
Near Sighted
|
|
|
| Solar Retinopathy |
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Oguchi Disease 1 |
|
Oguchi Disease-1
|
CSNBO1
|
|
Night Blindness, Congenital Stationary, Oguchi Type 1
|
Congenital Stationary Night Blindness Oguchi Type 1
|
|
Oguchi Disease
|
|
|
| Oguchi Disease 2 |
|
Oguchi Disease-2
|
CSNBO2
|
|
Night Blindness, Congenital Stationary, Oguchi Type 2
|
Congenital Stationary Night Blindness Oguchi Type 2
|
|
|
| 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
|
|
|
| Refractive Error |
|
|
| Chorioretinal Scar |
|
Chorioretinal Cicatrix
|
Cicatrix Of Choroid
|
|
Choroid Scar
|
Macula Scar
|
|
Macular Scarring
|
Retinal Cicatrix
|
|
Retinal Scar
|
|
|
| Cholera |
|
Vibrio Cholerae Infection
|
Cholera - Vibrio Cholerae
|
|
Cholera Due To Vibrio Cholerae
|
Vibrio Cholerae
|
|
Cholera Syndrome
|
Asiatic Cholera
|
|
Epidemic Cholera
|
|
|
| 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
|
|
|
| Pineocytoma |
|
Pinealoma
|
Pinealocytoma
|
|
Pineal Gland Neoplasm
|
Tumor Of The Pineal Region
|
|
|
| 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
|
|
|
| Myasthenic Syndrome, Congenital, 3a, Slow-Channel |
|
Congenital Myasthenic Syndrome 3a
|
CMS3A
|
|
Congenital Myasthenic Syndrome 3a, Slow-Channel
|
Myasthenic Syndrome, Congenital, Type 3a, Slow-Channel
|
|
|
| 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
|
|
|
| Microvascular Complications Of Diabetes 5 |
|
Diabetic Retinopathy
|
Microvascular Complications Of Diabetes, Susceptibility To, 5
|
|
MVCD5
|
Retinopathy, Diabetic
|
|
Diabetic Nephropathy
|
Retinopathy, Diabetic, Susceptibility To
|
|
Retinal Abnormality - Diabetes-Related
|
|
|
| Retinal Perforation |
|
Retinal Break
|
Retinal Perforations
|
|
Retinal Dialysis
|
Retinal Tear
|
|
Retinal Break Nos
|
Ruptured Retina
|
|
|
| Retinal Disease |
|
Retinal Diseases
|
Retinal Disorder
|
|
Retinal Disorders
|
|
|
| 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
|
|
|
| Red-Green Color Blindness |
|
Deutan Defect
|
Deuteranopia
|
|
Reduced Red-Green Discrimination
|
Color Blindness, Red-Green
|
|
Colorblindness, Partial, Deutan Series
|
|
|
| Eye Disease |
|
Eye Diseases
|
Abnormality Of The Eye
|
|
Toxoplasma Oculopathy
|
|
|
| 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
|
|
|
| Glucocorticoid Deficiency 1 |
|
Acth Resistance
|
Glucocorticoid Deficiency, Due To Acth Unresponsiveness
|
|
GCCD1
|
Familial Glucocorticoid Deficiency 1
|
|
Fgd1
|
Adrenal Unresponsiveness To Acth
|
|
Hereditary Unresponsiveness To Adrenocorticotropic Hormone
|
Isolated Glucocorticoid Deficiency
|
|
|
| Peripheral Retinal Degeneration |
|
Peripheral Degeneration Of Retina
|
Degeneration Of Retina Nos
|
|
Reticular Retinal Degeneration
|
Retinal Degeneration
|
|
|
| Choroid Disease |
|
Choroid Diseases
|
Abnormality Of The Choroid
|
|
|
| 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
|
|
|
| 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
|
|
|
| Sensory System Disease |
|
|
| Glaucoma, Primary Open Angle |
|
Glaucoma 1, Open Angle, E
|
Primary Open Angle Glaucoma
|
|
POAG
|
Adult-Onset Primary Open Angle Glaucoma
|
|
Chronic Simple Glaucoma
|
GLC1E
|
|
Primary Open Angle Glaucoma 1e
|
Glaucoma, Open Angle, Primary
|
|
|
| Achromatopsia |
|
Achm
|
Rod Monochromatism
|
|
Total Color Blindness
|
Rod Monochromacy
|
|
Monochromatism
|
Achromatism
|
|
Complete Or Incomplete Color Blindness
|
Pingelapese Blindness
|
|
Achromatopsia 1
|
Achromatopsia 2
|
|
Achromatopsia 3
|
|
|
| Vitreous Disease |
|
Disorder Of Vitreous Body
|
|
|
| Macular Retinal Edema |
|
Macular Edema
|
Macular Oedema
|
|
Macular Retinal Oedema
|
Macular Edema, Cystoid
|
|
|
| Sorsby Fundus Dystrophy |
|
SFD
|
Fundus Dystrophy, Pseudoinflammatory, Of Sorsby
|
|
Sorsby'S Fundus Dystrophy
|
Macular Dystrophy, Hemorrhagic
|
|
Hemorrhagic Macular Dystrophy
|
Pseudoinflammatory Fundus Dystrophy Of Sorsby
|
|
Sorsby'S Pseudoinflammatory Macular Dystrophy
|
Sorsby Pseudoinflammatory Fundus Dystrophy
|
|
Dystrophy, Fundus, Sorsby
|
|
|
| Colorblindness, Partial, Protan Series |
|
Protanopia
|
Red Color Blindness
|
|
Protan Defect
|
CBP
|
|
Red Colorblindness
|
Colorblindness, Protan
|
|
Color Blindness, Red
|
|
|
| Vitelliform Macular Dystrophy |
|
Best Disease
|
Juvenile-Onset Vitelliform Macular Dystrophy
|
|
Macular Dystrophy, Vitelliform
|
Best Macular Dystrophy
|
|
Vitelliform Dystrophy
|
|
|
| Leber Congenital Amaurosis 10 |
|
LCA10
|
Leber Congenital Amaurosis, Type 10
|
|
|
| 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
|
|
|
| Exudative Vitreoretinopathy 1 |
|
Retinopathy Of Prematurity
|
Retrolental Fibroplasia
|
|
EVR1
|
Criswick-Schepens Syndrome
|
|
Rop
|
Exudative Vitreoretinopathy, Familial, Autosomal Dominant
|
|
Fevr, Autosomal Dominant
|
Premature Retinopathy
|
|
Vitreoretinopathy, Exudative 1
|
Autosomal Dominant Familial Exudative Vitreoretinopathy
|
|
Fevr
|
Vitreoretinopathy, Exudative, Type 1
|
|
Retinopathy Of Prematurity Nos
|
Rlf- [Retrolental Fibroplasia]
|
|
Rop - [Retinopathy Of Prematurity]
|
Terry Syndrome
|
|
|
| Prolonged Electroretinal Response Suppression |
|
|
| Cone Dystrophy |
|
Retinal Cone Dystrophy
|
Dystrophy, Cone
|
|
Cone Dystrophy 3
|
|
|
| X-Linked Nephrogenic Diabetes Insipidus |
|
Nephrogenic Diabetes Insipidus Type 1
|
Doid:0081060
|
|
|
| Choroideremia |
|
CHM
|
Tcd
|
|
Progressive Tapetochoroidal Dystrophy
|
Choroidal Sclerosis
|
|
Tapetochoroidal Dystrophy, Progressive
|
Progressive Choroidal Atrophy
|
|
Tapetochoroidal Dystrophy
|
|
|
| Retinitis Pigmentosa 2 |
|
RP2
|
X-Linked Retinitis Pigmentosa 2
|
|
Xlrp2
|
Xlrp-2
|
|
Retinitis Pigmentosa-2
|
Retinitis Pigmentosa, Type 2
|
|
|
| Lens Disease |
|
|
| Retinal Vascular Occlusion |
|
Retinal Vasc. Occlusion
|
Occlusion Of Retinal Vessels
|
|
Retinal Obstruction
|
|
|
| Retinal Ischemia |
|
|
| Nephrogenic Diabetes Insipidus |
|
Vasopressin-Resistant Diabetes Insipidus
|
Diabetes Insipidus, Nephrogenic
|
|
Diabetes Insipidus Nephrogenic
|
Congenital Nephrogenic Diabetes Insipidus
|
|
Adh Resistant Diabetes Insipidus
|
Diabetes Insipidus Nephrogenic X-Linked
|
|
Diabetes Insipidus Nephrogenic Type 1
|
Adh-Resistant Diabetes Insipidus
|
|
Diabetes Insipidus Renalis
|
Ndi
|
|
Renal Diabetes Insipidus
|
Familial Nephrogenic Diabetes
|
|
Antidiuretic-Hormone-Resistant Diabetes Insipidus
|
Adiuretin-Resistant Diabetes Insipidus
|
|
Ndi - [Nephrogenic Diabetes Insipidus]
|
Diabetes Tenuifluus
|
|
Adh - [Antidiuretic-Hormone] Resistant Diabetes Insipidus
|
Hereditary Nephrogenic Diabetes Insipidus
|
|
Familial Nephrogenic Diabetes Insipidus
|
Primary Nephrogenic Diabetes Insipidus
|
|
|
| Usher Syndrome Type 2 |
|
Ush2
|
Usher Syndrome Type Ii
|
|
|
| Retinal Vascular Disease |
|
Retinal Vascular
|
Retinal Vascular Disorder
|
|
Retina Circulation Disorder
|
|
|
| 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
|
|
|
| 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 26 |
|
RP26
|
Retinitis Pigmentosa-26
|
|
Retinitis Pigmentosa, Type 26
|
|
|
| Uveal Disease |
|
|
| Transient Refractive Change |
|
|
| Retinitis Pigmentosa 7 |
|
Leber Congenital Amaurosis 18
|
RP7
|
|
Retinitis Pigmentosa 7, Digenic Form
|
Retinitis Pigmentosa 7 And Digenic Form
|
|
Retinitis Pigmentosa 7, Digenic
|
LCA18
|
|
Retinitis Pigmentosa 7 Digenic
|
|
|
| Major Depressive Disorder |
|
Seasonal Affective Disorder
|
Unipolar Depression
|
|
Depression
|
MDD
|
|
Depressive Disorder
|
Unipolar Depression, Susceptibility To
|
|
Major Depressive Disorder 1
|
Major Depressive Disorder, Response To Citalopram Therapy In
|
|
Major Depressive Disorder 2
|
Winter Depression
|
|
Single Major Depressive Episode
|
Sad
|
|
Clinical Depression
|
Major Depression
|
|
Depressive Syndrome
|
Major Depressive Disorder And Accelerated Response To Antidepressant Drug Treatment
|
|
Seasonal Affective Disorder, Susceptibility To
|
Recurrent Major Depression
|
|
Affective Disorder, Seasonal
|
Depression In A Seasonal Pattern
|
|
Depression
|
Seasonal
|
|
Major Depressive Disorder With A Seasonal Pattern
|
Seasonal Depression
|
|
Seasonal Mood Disorder
|
Mental Depression
|
|
Recurrent Major Depressive Episodes
|
|
|
| Nanophthalmos |
|
|
| 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
|
|
|
| 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
|
|
|
| Nephronophthisis |
|
Medullary Cystic Disease
|
Medullary Cystic Kidney
|
|
Nph
|
Nphp
|
|
Kidney Disease, Cystic, Medullary
|
|
|
| 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
|
|
|
| Bardet-Biedl Syndrome |
|
Bbs
|
Biedl-Bardet Syndrome
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
