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bn:04837845n
Noun Concept
EN
corneal opacification and other ocular anomalies  anterior segment dysgenesis  sclerocornea with other ocular anomalies
EN
Sclerocornea that has material basis in homozygous or compound heterozygous mutation in the PXDN gene on chromosome 2p25 and is characterized by corneal opacifiaction, cataract, microcornea, microphthalmia, and anterior segment dysgenesis Wikidata
Definitions
Relations
Sources
EN
Sclerocornea that has material basis in homozygous or compound heterozygous mutation in the PXDN gene on chromosome 2p25 and is characterized by corneal opacifiaction, cataract, microcornea, microphthalmia, and anterior segment dysgenesis Wikidata
IS A
genetic disease
eye disease
sclerocornea
monogenic disease
HAS KIND
anterior segment dysgenesis 7
HEALTH SPECIALTY
ophthalmology
Wikidata
EN
corneal opacification and other ocular anomalies
Wikidata Alias
EN
anterior segment dysgenesis, corneal opacification and other ocular anomalies, sclerocornea with other ocular anomalies

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