Developmental delay-overweight-facial dysmorphism-behavioral abnormalities syndrome
ORPHA:652487疾病暂无中文名
定义 英文原文（暂无中文）
A rare overgrowth/obesity syndrome characterized by mild developmental delay (notably speech delay), behaviour abnormalities (including autistic or attention deficit hyperactivity disorder features, hypersociability/ overfriendliness), overweight/obesity and mild dysmorphic features (including deep set eyes, broad bulbous nasal tip, large everted ears and thin upper lip). Other clinical features include variable and mild intellectual diability when present, broad short hands and feet.
基本事实
- 遗传方式
- 常染色体显性
相关基因 1
| 基因 | 名称 | 关联类型 |
|---|---|---|
| SRRM2 | serine/arginine repetitive matrix 2 | Disease-causing germline mutation(s) in |
外部标识与链接
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本页数据来源
- 疾病定义、同义词、基因、表型、流行病学：Orphanet（CC BY 4.0）
- 中文病名：Orphanet 中文包，冻结于 2020-06-01；本条目在该版本中无中文名
- 表型中文标签：HPO 简体中文翻译（CHPO 上游成果）