Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Formula: 18Target: 17Links: 42
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 1095
- Core Entity Id
- 1238
- Source Entity Count
- 1
- Preferred Name
- Microcephaly 20, Primary, Autosomal Recessive
- Name Cn
- 原发性常染色体隐性小头畸形20型
- Name Pinyin
- Yuan Fa Xing Chang Ran Se Ti Yin Xing Xiao Tou Ji Xing 20 Xing
- Name En
- Microcephaly 20, Primary, Autosomal Recessive
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Congenital Abnormality
- Disgenet Type
- disease
- Mesh Class
- Do Class
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- Disease Definition
- Version
- Suppressed
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Microcephaly 20, Primary, Autosomal Recessive
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS027557
Omim
617914
Dis Ge Net
C4693572
Umls Sty
T019
Etcm Disease
Microcephaly 20, Primary, Autosomal Recessive
Tcmbank Disease
2035
Itcmdb Generated
ITX-DISEASE-90F0592E7EA3
Attributes
Merged source attributes and domain-specific metadata.
Page Title
Disease Microcephaly 20, Primary, Autosomal Recessive Details page
Disease Type
disease
Umls Disease Type
Congenital Abnormality
Basic Information
Disease Name
Microcephaly 20, Primary, Autosomal Recessive
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Eye diseases;Mental diseases;Neuronal diseases
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Congenital Abnormality