Cohen syndrome (Q1107087)
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a rare genetic developmental disorder characterized by microcephaly, characteristic facial features, hypotonia, non-progressive intellectual deficit, myopia and retinal dystrophy, neutropenia and truncal obesity
- COHEN SYNDROME
- Pepper Syndrome
- COH1
- Chs1
- Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness
- COHEN SYNDROME; COH1
- Coh
- Chs1, Formerly
- Hypotonia, Obesity, and Prominent Incisors
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Cohen syndrome |
a rare genetic developmental disorder characterized by microcephaly, characteristic facial features, hypotonia, non-progressive intellectual deficit, myopia and retinal dystrophy, neutropenia and truncal obesity |
|
Statements
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759.89
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Identifiers
Cohen syndrome
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28 January 2022
Sitelinks
Wikipedia(11 entries)
- arwiki متلازمة كوهين
- bswiki Cohenov sindrom
- dewiki Cohen-Syndrom
- enwiki Cohen syndrome
- eswiki Síndrome de Cohen
- fiwiki Cohenin oireyhtymä
- frwiki Syndrome de Cohen
- itwiki Sindrome di Cohen
- plwiki Zespół Cohena
- trwiki Cohen sendromu
- zhwiki 科恩綜合症