DiseaseID 14493

1p36染色体缺失综合征

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: 1Formula: 11Target: 17Links: 35
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Record Fields

Scalar fields from the final disease record.

Disease Id
14493
Core Entity Id
72287
Source Entity Count
1
Preferred Name
Chromosome 1P36 Deletion Syndrome
Name Cn
1p36染色体缺失综合征
Name Pinyin
1p36 Ran Se Ti Que Shi Zong He Zheng
Name En
Chromosome 1P36 Deletion Syndrome
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Pathological Conditions, Signs and Symptoms
Do Class
genetic disease
Hpo Class
Mesh Class Name
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Hpo Class Name
Do Class Name
genetic disease
Disease Definition
Version
Suppressed

Names

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

Name
Chromosome 1P36 Deletion Syndrome
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS015972
Do Class
DOID:630
Dis Ge Net
C1842870
Umls Sty
T047
Me Sh Class
C16C23
Etcm Disease
Chromosome 1p36 Deletion Syndrome
Tcmbank Disease
18638
Itcmdb Generated
ITX-DISEASE-46A2FC00DF7A

Attributes

Merged source attributes and domain-specific metadata.

Page Title
Disease Chromosome 1p36 Deletion Syndrome Details page
Do Class Name
genetic disease
Disease Type
disease
Do Disease Class
genetic disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Chromosome 1p36 Deletion Syndrome
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Neuronal diseases
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Pathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Umls Semantic Type Name
Disease or Syndrome