DiseaseID 21734

髓鞘形成不良性脑白质营养不良10型

disease

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Relationship Network

Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.

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Disease: 1Target: 19Links: 24
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
21734
Core Entity Id
80481
Source Entity Count
1
Preferred Name
Leukodystrophy, Hypomyelinating, 10
Name Cn
髓鞘形成不良性脑白质营养不良10型
Name Pinyin
Sui Qiao Xing Cheng Bu Liang Xing Nao Bai Zhi Ying Yang Bu Liang 10 Xing
Name En
Leukodystrophy, Hypomyelinating, 10
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Do Class
disease of anatomical entity; genetic disease
Hpo Class
Mesh Class Name
Hpo Class Name
Do Class Name
genetic disease; disease of anatomical entity
Disease Definition
Version
v1
Suppressed
No

Names

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

Name
Leukodystrophy, Hypomyelinating, 10
Role
preferred
Name
HLD10
Role
alias
Name
Hypomyelinating Leukodystrophy 10
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS025737
Omim
616420
Umls
C4225332
Sym Map
SMDE01048
Do Class
DOID:630DOID:7
Dis Ge Net
C4225332
Umls Sty
T047
Etcm Disease
Leukodystrophy, Hypomyelinating, 10
Tcmbank Disease
472
Itcmdb Generated
ITX-DISEASE-AB87B93616BF

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0
Page Title
Disease Leukodystrophy, Hypomyelinating, 10 Details page
Do Class Name
genetic disease; disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entity; genetic disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Leukodystrophy, Hypomyelinating, 10
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Eye diseases;Neuronal diseases
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome