Eye Diseases, Hereditary

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.

Year introduced: 1990

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Do not include MeSH terms found below this term in the MeSH hierarchy.

Tree Number(s): C11.270, C16.320.290

MeSH Unique ID: D015785

Entry Terms:

• Hereditary Eye Diseases
• Eye Disease, Hereditary
• Hereditary Eye Disease

Previous Indexing:

• Eye Diseases/genetics (1966-1989)

All MeSH Categories
Diseases Category
Eye Diseases
Eye Diseases, Hereditary
Aicardi Syndrome
Albinism
Albinism, Ocular
Albinism, Oculocutaneous +
Chediak-Higashi Syndrome +
Aniridia
WAGR Syndrome
Choroideremia
Coloboma
CHARGE Syndrome
Mandibulofacial Dysostosis
Cone Dystrophy
Color Vision Defects
Cone-Rod Dystrophies
Corneal Dystrophies, Hereditary
Corneal Dystrophy, Juvenile Epithelial of Meesmann
Fuchs' Endothelial Dystrophy
Duane Retraction Syndrome
Familial Exudative Vitreoretinopathies
Graves Ophthalmopathy
Gyrate Atrophy
Leber Congenital Amaurosis
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
Optic Atrophy, Hereditary, Leber
Wolfram Syndrome
Optic Nerve Hypoplasia
Retinal Degeneration
Retinal Dysplasia
Retinitis Pigmentosa
Alstrom Syndrome
Bardet-Biedl Syndrome
Retinoblastoma
Stargardt Disease
Walker-Warburg Syndrome
Weill-Marchesani Syndrome

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Aicardi Syndrome
Albinism
Albinism, Ocular
Albinism, Oculocutaneous +
Piebaldism
Aniridia
WAGR Syndrome
Choroideremia
Cone-Rod Dystrophies
Corneal Dystrophies, Hereditary
Corneal Dystrophy, Juvenile Epithelial of Meesmann
Fuchs' Endothelial Dystrophy
Duane Retraction Syndrome
Familial Exudative Vitreoretinopathies
Graves Ophthalmopathy
Gyrate Atrophy
Optic Atrophies, Hereditary
Optic Atrophy, Autosomal Dominant
Optic Atrophy, Hereditary, Leber
Wolfram Syndrome
Optic Nerve Hypoplasia
Retinal Dysplasia
Retinitis Pigmentosa
Alstrom Syndrome
Usher Syndromes
Stargardt Disease
Vitelliform Macular Dystrophy
Weill-Marchesani Syndrome