Congenital Disorder

Eye Diseases, Hereditary

AMW:DIS:110040

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.

Pathology clinical

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Eye Diseases, Hereditary has parent Eye Diseases

Retinoblastoma has parent Eye Diseases, Hereditary

Weill-Marchesani Syndrome has parent Eye Diseases, Hereditary

Duane Retraction Syndrome has parent Eye Diseases, Hereditary

Optic Atrophies, Hereditary has parent Eye Diseases, Hereditary

Optic Nerve Hypoplasia has parent Eye Diseases, Hereditary

Aicardi Syndrome has parent Eye Diseases, Hereditary

Walker-Warburg Syndrome has parent Eye Diseases, Hereditary

Corneal Dystrophies, Hereditary has parent Eye Diseases, Hereditary

Aniridia has parent Eye Diseases, Hereditary

Coloboma has parent Eye Diseases, Hereditary

Familial Exudative Vitreoretinopathies has parent Eye Diseases, Hereditary

Retinal Dysplasia has parent Eye Diseases, Hereditary

Albinism has parent Eye Diseases, Hereditary

Choroideremia has parent Eye Diseases, Hereditary

Cone Dystrophy has parent Eye Diseases, Hereditary

Cone-Rod Dystrophies has parent Eye Diseases, Hereditary

Graves Ophthalmopathy has parent Eye Diseases, Hereditary

Gyrate Atrophy has parent Eye Diseases, Hereditary

Leber Congenital Amaurosis has parent Eye Diseases, Hereditary

Retinal Degeneration has parent Eye Diseases, Hereditary

Retinitis Pigmentosa has parent Eye Diseases, Hereditary

Stargardt Disease has parent Eye Diseases, Hereditary

Vitelliform Macular Dystrophy has parent Eye Diseases, Hereditary

Eye Diseases, Hereditary has parent Genetic Diseases, Inborn

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