DiseaseID 18669

中心凹发育不良2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: 1Symptom: 3Target: 17Links: 27
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Record Fields

Scalar fields from the final disease record.

Disease Id
18669
Core Entity Id
77101
Source Entity Count
1
Preferred Name
Foveal Hypoplasia 2
Name Cn
中心凹发育不良2型
Name Pinyin
Zhong Xin Ao Fa Yu Bu Liang 2 Xing
Name En
Foveal Hypoplasia 2
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Do Class
Hpo Class
Mesh Class Name
Hpo Class Name
Do Class Name
Disease Definition
Version
v1
Suppressed
No

Names

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

Name
Foveal Hypoplasia 2
Role
preferred
Name
FHONDA
Role
alias
Name
FOVEAL HYPOPLASIA 2 WITH OPTIC NERVE DECUSSATION DEFECTS AND ANTERIOR SEGMENT DYSGENESIS WITHOUT ALBINISM
Role
alias
Name
FOVEAL HYPOPLASIA 2 WITH OR WITHOUT OPTIC NERVE MISROUTING AND/OR ANTERIOR SEGMENT DYSGENESIS
Role
alias
Name
FVH2
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS022260
Umls
C3807873
Sym Map
SMDE00529
Dis Ge Net
C3807873
Umls Sty
T047
Etcm Disease
Foveal Hypoplasia 2
Tcmbank Disease
22050
Itcmdb Generated
ITX-DISEASE-1ECAB725767DITX-DISEASE-43B54D3E79D3

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0
Page Title
Disease Foveal Hypoplasia 2 Details page
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Foveal Hypoplasia 2
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Eye diseases;Neuronal diseases
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome