DiseaseID 18746
家族性发作性疼痛综合征3型
disease
NCI2016_02D:A rare, autosomal dominant disorder caused by mutation in the SCN11A gene. It is characterized by intense episodic pain mainly affecting the distal lower extremities in early childhood. The pain diminishes wi
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Herb: 12Symptom: 1Target: 17Links: 37
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 18746
- Core Entity Id
- 77192
- Source Entity Count
- 1
- Preferred Name
- Episodic Pain Syndrome, Familial, 3
- Name Cn
- 家族性发作性疼痛综合征3型
- Name Pinyin
- Jia Zu Xing Fa Zuo Xing Teng Tong Zong He Zheng 3 Xing
- Name En
- Episodic Pain Syndrome, Familial, 3
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Pathological Conditions, Signs and Symptoms
- Do Class
- Hpo Class
- Mesh Class Name
- Pathological Conditions, Signs and Symptoms
- Hpo Class Name
- Do Class Name
- Disease Definition
- NCI2016_02D:A rare, autosomal dominant disorder caused by mutation in the SCN11A gene. It is characterized by intense episodic pain mainly affecting the distal lower extremities in early childhood. The pain diminishes with age.
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Episodic Pain Syndrome, Familial, 3
Role
preferred
Name
FEPS3
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS022389
Omim
615552
Umls
C3809899
Sym Map
SMDE01030
Dis Ge Net
C3809899
Umls Sty
T047
Me Sh Class
C23
Etcm Disease
Episodic Pain Syndrome, Familial, 3
Tcmbank Disease
25927
Itcmdb Generated
ITX-DISEASE-EC0F39DEADFF
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease Episodic Pain Syndrome, Familial, 3 Details page
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Episodic Pain Syndrome, Familial, 3
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Neuronal diseases
Disease Definition
NCI2016_02D:A rare, autosomal dominant disorder caused by mutation in the SCN11A gene. It is characterized by intense episodic pain mainly affecting the distal lower extremities in early childhood. The pain diminishes with age.
Me Sh Disease Class
Pathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Pathological Conditions, Signs and Symptoms
Umls Semantic Type Name
Disease or Syndrome