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arcus senilispars planitisBlau syndromeangioid streaksosteogenesis imperfecta-retinopathy-seizures-intellectual disability syndromeblindness-scoliosis-arachnodactyly syndromeMicrovascular complications of diabetes, susceptibility to, 2Microvascular complications of diabetes, susceptibility to, 5Microvascular complications of diabetes, susceptibility to, 7microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndromemyopia 25, autosomal dominant; MYP25rare genetic palpebral, lacrimal system and conjunctival diseaserare genetic refraction anomalyhereditary eye tumorchondroectodermal dysplasia with night blindnesshereditary glaucomaglobal developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndromedevelopmental defect of the eyerare palpebral, lacrimal system and conjunctival diseasesyndromic glaucomagenetic vitreous-retinal diseasehereditary optic neuropathygenodermatosis with ocular featuresconnective tissue disease with eye involvementectodermal malformation syndrome associated with ocular featuresmetabolic disease associated with ocular featurescalloso-genital dysplasiakeratoconusretinal detachmentCINCA syndrome
P279
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P279
description
form of eye disease that is both rare and inborn
@en
name
enfermedad genética de los ojos, rara
@es
malaltia genètica dels ulls, rara
@ca
rare genetic eye disease
@en
type
label
enfermedad genética de los ojos, rara
@es
malaltia genètica dels ulls, rara
@ca
rare genetic eye disease
@en
altLabel
Rare genetic ophthalmologic disease
@en
prefLabel
enfermedad genética de los ojos, rara
@es
malaltia genètica dels ulls, rara
@ca
rare genetic eye disease
@en
P279
P1550
P2888
P5270
MONDO:0015107