OMOP Concept 37472705
P3H2 gene related high myopia, cataract, vitreoretinal degeneration
StandardConditionSNOMED1381540004Disorder
Maps from
0
Descendants
0
Valid from
1 Dec 2025
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for P3H2 gene related high myopia, cataract, vitreoretinal degeneration across source vocabularies.
- LEPREL1 gene related high myopia, cataract, vitreoretinal degeneration
- miopía alta, cataratas y degeneración vitreorretiniana relacionadas con el gen de prolil 3-hidroxilasa 2
- miopía alta, cataratas y degeneración vitreorretiniana relacionadas con el gen de prolil 3-hidroxilasa 2 (trastorno)
- miopía alta, cataratas y degeneración vitreorretiniana relacionadas con el gen LEPREL1
- miopía alta, cataratas y degeneración vitreorretiniana relacionadas con el gen P3H2
- Prolyl 3-hydroxylase 2 gene related high myopia, cataract, vitreoretinal degeneration
- Prolyl 3-hydroxylase 2 gene related-high myopia, cataract, vitreoretinal degeneration
- Prolyl 3-hydroxylase 2 gene related high myopia, cataract, vitreoretinal degeneration (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(54)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Cataract
- 1Connective tissue hereditary disorder
- 1Rare isolated myopia
- 1Vitreoretinal degeneration
- 2Atrophic retina
- 2Atrophy of soft tissue of orbit
- 2Autosomal hereditary disorder
- 2Cataract finding
- 2Degenerative disorder of eye
- 2Disorder of connective tissue
- 2Disorder of lens
- 2Hereditary disease
- 2Hereditary disorder of the visual system
- 2Lesion of eye
- 2Peripheral retinal degeneration
- 2Severe myopia
- 2Vitreous degeneration
- 3Anomaly of eye
- 3Atrophy of globe of eye
- 3Crystalline lens finding
- 3Degeneration of retina
- 3Degenerative disorder
- 3Disease
- 3Disorder of anterior segment of eye
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