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Term:
Retinal Aplasia
(DOID:9006874)
Annotations:
Rat: (0)
Mouse: (0)
Human: (0)
Chinchilla: (0)
Bonobo: (0)
Dog: (0)
Squirrel: (0)
Pig: (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 with Oculomotor Apraxia Type 4
Ataxia-Microcephaly-Cataract Syndrome
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 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