DiseaseID 14551

纽芬兰杆锥细胞营养不良

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: 1Links: 4
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Record Fields

Scalar fields from the final disease record.

Disease Id
14551
Core Entity Id
72354
Source Entity Count
1
Preferred Name
Newfoundland Rod-Cone Dystrophy
Name Cn
纽芬兰杆锥细胞营养不良
Name Pinyin
Niu Fen Lan Gan Zhui Xi Bao Ying Yang Bu Liang
Name En
Newfoundland Rod-Cone Dystrophy
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
Do Class
disease of anatomical entity; genetic disease
Hpo Class
Mesh Class Name
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Hpo Class Name
Do Class Name
genetic disease; disease of anatomical entity
Disease Definition
Version
v1,v2
Suppressed
No

Names

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

Name
Newfoundland Rod-Cone Dystrophy
Role
preferred
Name
NFRCD
Role
alias
Name
Newfoundland Cone-Rod Dystrophy
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS016057
Omim
607476
Umls
C1843815
Sym Map
SMDE01293
Do Class
DOID:630DOID:7
Dis Ge Net
C1843815
Umls Sty
T047
Me Sh Class
C11C16
Tcmbank Disease
17215

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
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
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Umls Semantic Type Name
Disease or Syndrome