DiseaseID 17282

视神经萎缩7型(疾病)

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: 1Links: 1
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Record Fields

Scalar fields from the final disease record.

Disease Id
17282
Core Entity Id
75490
Source Entity Count
1
Preferred Name
Optic Atrophy 7 (Disorder)
Name Cn
视神经萎缩7型(疾病)
Name Pinyin
Shi Shen Jing Wei Suo 7 Xing ( Ji Bing )
Name En
Optic Atrophy 7 (Disorder)
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Eye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Do Class
disease of anatomical entity; genetic disease
Hpo Class
Mesh Class Name
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases
Hpo Class Name
Do Class Name
genetic disease; disease of anatomical entity
Disease Definition
Version
Suppressed

Names

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

Name
Optic Atrophy 7 (Disorder)
Role
preferred
Name
Optic Atrophy 7
Role
alias
Name
Optic Atrophy 7 With Or Without Auditory Neuropathy
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS019974
Omim
612989
Do Class
DOID:630DOID:7
Dis Ge Net
C2751812
Umls Sty
T047
Me Sh Class
C10C11C16
Tcmbank Disease
10250

Attributes

Merged source attributes and domain-specific metadata.

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
Me Sh Disease Class
Eye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases
Umls Semantic Type Name
Disease or Syndrome