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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
eye disease +     
genetic disease +     
Adrenocortical Hypofunction, Chronic Primary Congenital 
adrenocorticotropic hormone deficiency  
advanced sleep phase syndrome 3  
age related macular degeneration 8  
agenesis of corpus callosum, cardiac, ocular, and genital syndrome  
Alpha-2-Deficient Collagen Disease 
amblyopia +   
ancylostomiasis +  
Aquaporin 1 Deficiency  
Asthenopia  
ataxic cerebral palsy 
atrial heart septal defect 3  
atrial heart septal defect 4  
autoimmune lymphoproliferative syndrome +   
baylisascariasis 
blindness +   
BOCKENHEIMER SYNDROME  
brachydactyly type A1B 
brachydactyly type A1C  
brachydactyly type A1D  
brachydactyly type B1  
brachydactyly type B2  
brachydactyly type E1  
brachydactyly type E2  
CADASIL +   
CAKUT2  
cataract 25 
cataract 26 multiple types 
cataract 27  
cataract 28 
Cenani-Lenz syndactyly syndrome  
Cerebellar, Ocular, Craniofacial, and Genital Syndrome  
chromosomal disease +   
Cogan syndrome +   
complex cortical dysplasia with other brain malformations 1  
complex cortical dysplasia with other brain malformations 2  
complex cortical dysplasia with other brain malformations 3  
complex cortical dysplasia with other brain malformations 4  
complex cortical dysplasia with other brain malformations 5  
complex cortical dysplasia with other brain malformations 6  
Congenital Hepatic Fibrosis  
Congenital Pain Insensitivity +   
conjunctival disease +   
corneal disease +   
cysticercosis +  
desquamative interstitial pneumonia  
dipetalonemiasis 
Dwarfism +   
Encephalocraniocutaneous Lipomatosis  
Eye Abnormalities +   
eye accommodation disease +  
eye adnexa disease +   
eye degenerative disease +   
Eye Hemorrhage +   
Eye Infections +   
Eye Injuries +   
Eye Manifestations +   
Eye Neoplasms +   
eyelid disease +   
Familial Cirrhosis +   
Familial Dysalbuminemic Hyperthyroxinemia  
Familial Hemophagocytic Lymphohistiocytoses +   
familial hypertrophic cardiomyopathy +   
Familial Lipochrome Histiocytosis 
Familial Mixed Cryoglobulinemia  
Familial Temporal Epilepsy +   
frontotemporal dementia and/or amyotrophic lateral sclerosis 3  
frontotemporal dementia and/or amyotrophic lateral sclerosis 4  
fundus dystrophy +   
Genetic Skin Diseases +   
glaucoma +   
globe disease +   
gonorrhea +  
Hereditary Bilateral Parotidomegaly 
Hereditary Epistaxis 
Hereditary Eye Diseases +   
Transmission of gene defects or chromosomal aberrations/abnormalities which are expressed in extreme variation in the structure or function of the eye. These may be evident at birth, but may be manifested later with progression of the disorder.
hereditary lymphedema +   
Hereditary Neoplastic Syndromes +   
Hereditary Sensorimotor Neuropathy with Upper Motor Neuron, Visual Pathway and Autonomic Disturbance 
Hernandez Fragoso Syndrome 
inherited metabolic disorder +   
Isolated Prolactin Deficiency 
Kallmann syndrome +   
lacrimal apparatus disease +   
Laminopathies +   
lens disease +   
leprosy +   
loiasis 
Marfan syndrome +   
microphthalmia +   
Mollica-Pavone-Antener Syndrome 
monogenic disease +   
MORM Syndrome  
Nervous System Heredodegenerative Disorders +   
NEURODEVELOPMENTAL DISORDER WITH VISUAL DEFECTS AND BRAIN ANOMALIES  
NEURODEVELOPMENTAL, JAW, EYE, AND DIGITAL SYNDROME  
Neuromuscular Oculoauditory Syndrome  
Nonimmune Chronic Idiopathic Neutropenia, Adult  
ocular hypertension +   
ocular hypotension +   
ocular motility disease +   
Ocular Neovascularization +   
ocular sarcoidosis  
ophthalmia nodosa 
ophthalmomyiasis 
optic nerve disease +   
orbital disease +   
philophthalmiasis 
polygenic disease +   
primary hypertrophic osteoarthropathy +   
progressive familial intrahepatic cholestasis +   
pupil disease +   
refractive error +   
retinal disease +   
Sacral Agenesis with Vertebral Anomalies  
scleral disease +   
scotoma +   
toxocariasis +   
uveal disease +   
Vision Disorders +   
visual pathway disease +   
vitreous detachment +   
vitreous disease +   
yellow nail syndrome +  
 achromatopsia 4  
 Achromatopsia 5  
 Acrootoocular Syndrome 
 Aicardi syndrome  
 Alacrima +   
 Albinism +   
 aniridia +   
 ataxia with oculomotor apraxia type 3  
 Ataxia-Microcephaly-Cataract Syndrome 
 ataxia-oculomotor apraxia type 4  
 basal laminar drusen  
 bestrophinopathy  
 Bothnia retinal dystrophy  
 bradyopsia +   
 cataract 17 multiple types  
 cataract 22 multiple types  
 cataract 35 
 Cataract, Pulverulent 
 Cavitary Optic Disc Anomalies  
 Cholestasis with Gallstone, Ataxia, and Visual Disturbance 
 Choroideremia +   
 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 +   
 Duane retraction syndrome +   
 enhanced S-cone syndrome  
 exudative vitreoretinopathy +   
 familial benign fleck retina  
 Floriform Cataract 
 Foveal Hypoplasia +   
 Foveal Hypoplasia with Anterior Segment Anomalies 
 Glaucoma 1, Open Angle, P  
 Graves ophthalmopathy  
 Grouped Pigmentation of the Macula 
 gyrate atrophy +   
 hereditary night blindness +   
 Hereditary Optic Atrophies +   
 hereditary retinal dystrophy +   
 High Hyperopia  
 Histiocytic Dermatoarthritis 
 Iris Pigment Epithelium Anomalies 
 Joubert syndrome 8  
 Leber congenital amaurosis +   
 megalocornea +   
 Microcephaly and Chorioretinopathy +   
 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  
 PORETTI-BOLTSHAUSER SYNDROME  
 primary congenital glaucoma +   
 pseudopapilledema 
 Radial Drusen, Autosomal Dominant  
 renal hypomagnesemia 5 with ocular involvement  
 Retinal Aplasia 
 Retinal Dysplasia +   
 Retinal Dystrophy, Early Onset Severe +   
 retinitis pigmentosa +   
 Retinohepatoendocrinologic Syndrome 
 Rhegmatogenous Retinal Detachment, Autosomal Dominant  
 Spondyloocular Syndrome, Autosomal Recessive  
 Stickler Syndrome, Type I, Nonsyndromic Ocular  
 Vascular Hyalinosis 
 vitelliform macular dystrophy +   
 Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia  
 Walker-Warburg syndrome +   
 Weill-Marchesani syndrome +   
 X-Linked Macular Dystrophy +   

Synonyms
Exact Synonyms: Hereditary Eye Disease
Primary IDs: MESH:D015785
Definition Sources: MESH:D015785

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