DiseaseID 30687

常染色体显性遗传罗兰多癫痫、智力障碍和言语运用障碍

Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, Autosomal Dominant

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Disease: 1Symptom: 4Target: 5Links: 9

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Scalar fields from the final disease record.

Disease Id: 30687
Core Entity Id: 123255
Source Entity Count: 1
Preferred Name: Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, Autosomal Dominant
Name Cn: 常染色体显性遗传罗兰多癫痫、智力障碍和言语运用障碍
Name Pinyin: Chang Ran Se Ti Xian Xing Yi Chuan Luo Lan Duo Dian Xian 、 Zhi Li Zhang Ai He Yan Yu Yun Yong Zhang Ai
Name En: Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, Autosomal Dominant
Name Latin
Bilingual Status: complete
Disease Type
Umls Disease Type
Disgenet Type
Mesh Class
Do Class
Hpo Class
Mesh Class Name
Hpo Class Name
Do Class Name
Disease Definition
Version: v2
Suppressed: No

Preferred names, aliases, and source labels retained in the final schema.

Name

Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, Autosomal Dominant

Role

preferred

Source

SymMap_v2

Preferred

Yes

Trusted external identifiers retained for this final record.

Sym Map

SMDE12910

Merged source attributes and domain-specific metadata.

Version

Suppress