DiseaseID 26386

常染色体隐性遗传原发性小头畸形1型

Microcephaly 1, Primary, Autosomal Recessive

Back to Browse

Relationship Network

Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.

Click a node to open it in a new tab
Disease: 1Symptom: 4Target: 19Links: 28
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
26386
Core Entity Id
118954
Source Entity Count
1
Preferred Name
Microcephaly 1, Primary, Autosomal Recessive
Name Cn
常染色体隐性遗传原发性小头畸形1型
Name Pinyin
Chang Ran Se Ti Yin Xing Yi Chuan Yuan Fa Xing Xiao Tou Ji Xing 1 Xing
Name En
Microcephaly 1, Primary, Autosomal Recessive
Name Latin
Bilingual Status
complete
Disease Type
Umls Disease Type
Disgenet Type
Mesh Class
Do Class
Hpo Class
Mesh Class Name
Hpo Class Name
Do Class Name
Disease Definition
Version
v1,v2
Suppressed
No

Names

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

Name
Microcephaly 1, Primary, Autosomal Recessive
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Umls
C1855081
Sym Map
SMDE03213
Etcm Disease
Microcephaly 1, Primary, Autosomal Recessive
Itcmdb Generated
ITX-DISEASE-75F9E14242B3

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Page Title
Disease Microcephaly 1, Primary, Autosomal Recessive Details page
Basic Information
Disease Name
Microcephaly 1, Primary, Autosomal Recessive
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Eye diseases;Mental diseases;Neuronal diseases