Lenz microphthalmia syndrome
human disease
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Lenz microphthalmia syndrome
Summary
Lenz microphthalmia syndrome is a hereditary disorder[1]. It draws 119 Wikipedia views per month (hereditary_disorder category, ranking #11 of 25).[2]
Key Facts
- Lenz microphthalmia syndrome's instance of is recorded as hereditary disorder[3].
- Lenz microphthalmia syndrome's instance of is recorded as developmental defect during embryogenesis[4].
- Lenz microphthalmia syndrome's instance of is recorded as rare disease[5].
- Lenz microphthalmia syndrome's instance of is recorded as class of disease[6].
- Lenz microphthalmia syndrome is a type of syndromic microphthalmia[7].
- Lenz microphthalmia syndrome is a type of X-linked disease[8].
- Lenz microphthalmia syndrome's ICD-9-CM is recorded as 759.89[9].
- Lenz microphthalmia syndrome's genetic association is recorded as NAA10[10].
- Lenz microphthalmia syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_568[11].
- Lenz microphthalmia syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111799[12].
- Lenz microphthalmia syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111799[13].
Why It Matters
Lenz microphthalmia syndrome draws 119 Wikipedia views per month (hereditary_disorder category, ranking #11 of 25).[2] It is known by 13 alternative names across languages and contexts.[14]