Welcome
{{ username}}
Message Center
{{ messageCount }} Messages
Go to Message Center
Watched Genes
{{$index + 1}}.
{{ watchedObject.symbol }} (RGD ID:{{watchedObject.rgdId}})
Modify Subscription
Unsubscribe
Watched Ontology Terms
{{$index + 1}}.
{{ watchedTerm.term }} ({{watchedTerm.accId}})
Modify Subscription
Unsubscribe
{{gene.symbol}}:
{{ gene.description }}
×
Save List to My RGD
Create Name:
Description:
You must be logged in to use this feature
{{ loginError }}
{{ watchLinkText }}
Select categories you would like to watch. Updates to this gene will be sent to {{ username }}
{{geneWatchAttr}}
Analyze
Gene
Strain
QTL
List
×
Gene Annotator (Functional Annotation)
unavailable
Gene Annotator (Annotation Distribution)
unavailable
Variant Visualizer (Genomic Variants)
unavailble
Variant Visualizer (Genomic Variants)
unavailable
Gene Annotator (Functional Annotation)
Gene Annotator (Annotation Distribution)
Variant Visualizer (Genomic Variants)
InterViewer (Protein-Protein Interactions)
unavailable
Gviewer (Genome Viewer)
unavailable
Variant Visualizer (Damaging Variants) unavailble
Variant Visualizer (Damaging Variants)
unavailable
InterViewer (Protein-Protein Interactions)
GViewer (Genome Viewer)
Variant Visualizer (Damaging Variants)
Gene Annotator (Annotation Comparison)
unavailable
OLGA (Gene List Generator)
unavailable
Gene Annotator (Annotation Comparison)
OLGA (Gene List Generator)
Excel (Download)
MOET (Multi-Ontology Enrichement)
unavailable
GOLF (Gene-Ortholog Location Finder)
unavailable
MOET (Multi-Ontology Enrichement)
GOLF (Gene-Ortholog Location Finder)
x
Send Message
x
Send us a Message
Your email
Message
Send
Submit Data
|
Help
|
Video Tutorials
|
News
|
Publications
|
Download
|
REST API
|
Citing RGD
|
Contact
Home
Search RGD
Grant Resources
Citing RGD
About Us
Contact Us
Data
Genes
Variants
Community Projects
QTLs
Strains
Markers
Genome Information
Ontologies
Cell Lines
References
Download
Submit Data
Analysis & Visualization
OntoMate (Literature Search)
JBrowse (Genome Browser)
Synteny Browser (VCMap)
Variant Visualizer
Multi-Ontology Enrichment (MOET)
Gene-Ortholog Location Finder (GOLF)
InterViewer (Protein-Protein Interactions)
PhenoMiner (Quatitative Phenotypes)
Gene Annotator
OLGA (Gene List Generator)
AllianceMine
GViewer (Genome Viewer)
Diseases
Aging & Age-Related Disease
Cancer & Neoplastic Disease
Cardiovascular Disease
Coronavirus Disease
Developmental Disease
Diabetes
Hematologic Disease
Immune & Inflammatory Disease
Infectious Disease
Liver Disease
Neurological Disease
Obesity & Metabolic Syndrome
Renal Disease
Respiratory Disease
Sensory Organ Disease
Phenotypes & Models
Find Models
new
Genetic Models
Autism Models
Rat PhenoMiner (Quantitative Phenotypes)
Chinchilla PhenoMiner
Expected Ranges (Quantitative Phenotype)
PhenoMiner Term Comparison
Hybrid Rat Diversity Panel
Phenotypes
Phenotypes in Other Animal Models
Animal Husbandry
Strain Medical Records
Phylogenetics
Strain Availability
Calendar
Rats 101
Submissions
Photo Archive
Pathways
Community
Rat Community Forum
Directory of Rat Laboratories
Video Tutorials
News
RGD Publications
RGD Presentations Archive
Nomenclature Guidelines
Resource Links
Laboratory Resources
Employment Resources
Advanced Search (OLGA)
Ontology Browser
Term:
Retinal Aplasia
(DOID:9006874)
Annotations:
Rat: (0)
Mouse: (0)
Human: (0)
Chinchilla: (0)
Bonobo: (0)
Dog: (0)
Squirrel: (0)
Pig: (0)
Naked Mole-rat: (0)
Green Monkey: (0)
Parent Terms
Term With Siblings
Child Terms
blindness
+
Hereditary Eye Diseases
+
retinal disease
+
achromatopsia 4
Achromatopsia 5
Acrootoocular Syndrome
Aicardi syndrome
Al Gazali Sabrinathan Nair Syndrome
Alacrima
+
Aland Island eye disease
Albinism
+
Amaurosis Fugax
angioid streaks
+
aniridia
+
ataxia with oculomotor apraxia type 3
Ataxia-Microcephaly-Cataract Syndrome
ataxia-oculomotor apraxia type 4
Ausems Wittebol-Post Hennekam Syndrome
basal laminar drusen
bestrophinopathy
Bietti crystalline corneoretinal dystrophy
Bothnia retinal dystrophy
bradyopsia
+
cataract 17 multiple types
cataract 22 multiple types
cataract 35
Cataract, Pulverulent
Cavitary Optic Disc Anomalies
Central Serous Chorioretinopathy
Cholestasis with Gallstone, Ataxia, and Visual Disturbance
chorioretinal scar
+
Choroideremia
+
color blindness
+
cone dystrophy
+
cone-rod dystrophy
+
Congenital Alacrima
+
congenital fibrosis of the extraocular muscles 1
congenital fibrosis of the extraocular muscles 2
congenital fibrosis of the extraocular muscles 3A
congenital fibrosis of the extraocular muscles 3C
congenital fibrosis of the extraocular muscles 5
Congenital Mydriasis
+
Cornea Plana 1
Cornea Plana 2
corneal dystrophy
+
cortical blindness
+
Deaf-Blind Disorders
+
distal arthrogryposis type 5
Duane retraction syndrome
+
enhanced S-cone syndrome
exudative vitreoretinopathy
+
familial benign fleck retina
Floriform Cataract
FLOTCH Syndrome
Foveal Hypoplasia
+
foveal hypoplasia 1
foveal hypoplasia 2
Foveal Hypoplasia with Anterior Segment Anomalies
fundus albipunctatus
Glaucoma 1, Open Angle, P
Graves ophthalmopathy
Grouped Pigmentation of the Macula
gyrate atrophy
+
Hemianopsia
hereditary night blindness
+
Hereditary Optic Atrophies
+
hereditary retinal dystrophy
+
High Hyperopia
Histiocytic Dermatoarthritis
hypertensive retinopathy
Iris Hypoplasia and Glaucoma
Iris Pigment Epithelium Anomalies
Joubert syndrome 8
Leber congenital amaurosis
+
megalocornea
+
Microcephaly and Chorioretinopathy
+
Microcephaly Microphthalmos Blindness
Microcephaly with Chorioretinopathy, Autosomal Dominant
neovascular inflammatory vitreoretinopathy
nerve fibre bundle defect
night blindness
+
Norrie disease
Omphalocele, Diaphragmatic Hernia, and Radial Ray Defects
Ophthalmomandibulomelic Dysplasia
Peripapillary Atrophy, Beta Type
Persistent Hyperplastic Primary Vitreous, Autosomal Dominant
Persistent Hyperplastic Primary Vitreous, Autosomal Recessive
pigmented paravenous chorioretinal atrophy
Polycystic Kidney, Cataract, and Congenital Blindness
PORETTI-BOLTSHAUSER SYNDROME
primary congenital glaucoma
+
pseudopapilledema
Radial Drusen, Autosomal Dominant
Rambaud Galian Syndrome
Ramos Arroyo Clark Syndrome
renal hypomagnesemia 5 with ocular involvement
Retina Reperfusion Injury
Retinal Aplasia
retinal arterial tortuosity
retinal artery occlusion
+
retinal degeneration
+
retinal detachment
+
Retinal Dysplasia
+
retinal dystrophy with leukodystrophy
Retinal Dystrophy, Early Onset Severe
+
retinal edema
+
Retinal Hemorrhage
+
Retinal Neoplasms
+
Retinal Neovascularization
retinal perforation
+
retinal vascular disease
+
retinal vasculopathy with cerebral leukodystrophy
retinitis
+
retinitis pigmentosa
+
Retinohepatoendocrinologic Syndrome
retinopathy of prematurity
+
Rhegmatogenous Retinal Detachment, Autosomal Dominant
Rodrigues Blindness
Roifman Syndrome
rubeosis iridis
Scoliosis, Arachnodactyly, and Blindness
Sickle Cell Retinopathy
Spondyloocular Syndrome, Autosomal Recessive
Stickler Syndrome, Type I, Nonsyndromic Ocular
Vascular Hyalinosis
visual impairment and progressive phthisis bulbi
vitelliform macular dystrophy
+
Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia
Walker-Warburg syndrome
+
Webb-Dattani Syndrome
Weill-Marchesani syndrome
+
X-Linked Macular Dystrophy
+
Yemenite Deaf-Blind Hypopigmentation Syndrome
Synonyms
Exact Synonyms:
Amaurosis Congenita
Primary IDs:
MESH:C566720
Alternate IDs:
OMIM:179900