DiseaseID 6176
致死性家族性失眠症
disease
NCI2016_02D:A very rare autosomal dominant inherited sleep disorder caused by a mutation in the gene responsible for the prion protein. It affects individuals usually in their fourth decade. Its initial manifestation is
Relationship Network
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Disease: 1Formula: 6Herb: 12Symptom: 11Target: 19Links: 53
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 6176
- Core Entity Id
- 62791
- Source Entity Count
- 1
- Preferred Name
- Fatal Familial Insomnia
- Name Cn
- 致死性家族性失眠症
- Name Pinyin
- Zhi Si Xing Jia Zu Xing Shi Mian Zheng
- Name En
- Fatal Familial Insomnia
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Infections; Nervous System Diseases
- Do Class
- disease of anatomical entity
- Hpo Class
- Mesh Class Name
- Infections; Nervous System Diseases
- Hpo Class Name
- Do Class Name
- disease of anatomical entity
- Disease Definition
- NCI2016_02D:A very rare autosomal dominant inherited sleep disorder caused by a mutation in the gene responsible for the prion protein. It affects individuals usually in their fourth decade. Its initial manifestation is difficulty in falling asleep. It is followed by complete inability to sleep. Patients develop deterioration of their mental and motor functions and die soon after the first symptoms appear, because of the total absence of sleep.|MSH2017_2016_08_12:An autosomal dominant disorder characterized by degeneration of the THALAMUS and progressive insomnia. It is caused by a mutation in the prion protein (PRIONS).
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Fatal Familial Insomnia
Role
preferred
Name
FFI
Role
alias
Name
INSOMNIA, FATAL FAMILIAL
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS004323
Me Sh
D034062
Omim
600072
Umls
C0206042
Icd10
A81.83
Sym Map
SMDE03170
Do Class
DOID:7
Dis Ge Net
C0206042
Umls Sty
T047
Me Sh Class
C01C10
Etcm Disease
Fatal Familial Insomnia
Tcmbank Disease
28959
Itcmdb Generated
ITX-DISEASE-AA9F57C2C2EB
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease Fatal Familial Insomnia Details page
Do Class Name
disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entity
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Fatal Familial Insomnia
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Mental diseases;Neuronal diseases
Disease Definition
NCI2016_02D:A very rare autosomal dominant inherited sleep disorder caused by a mutation in the gene responsible for the prion protein. It affects individuals usually in their fourth decade. Its initial manifestation is difficulty in falling asleep. It is followed by complete inability to sleep. Patients develop deterioration of their mental and motor functions and die soon after the first symptoms appear, because of the total absence of sleep.|MSH2017_2016_08_12:An autosomal dominant disorder characterized by degeneration of the THALAMUS and progressive insomnia. It is caused by a mutation in the prion protein (PRIONS).
Me Sh Disease Class
Infections; Nervous System Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Infections; Nervous System Diseases
Umls Semantic Type Name
Disease or Syndrome