DiseaseID 26419

颅骨干骺端发育不良,常染色体隐性

Craniometaphyseal Dysplasia, Autosomal Recessive

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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: 5Herb: 2Symptom: 4Target: 18Links: 35
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Record Fields

Scalar fields from the final disease record.

Disease Id
26419
Core Entity Id
118987
Source Entity Count
1
Preferred Name
Craniometaphyseal Dysplasia, Autosomal Recessive
Name Cn
颅骨干骺端发育不良,常染色体隐性
Name Pinyin
Lu Gu Gan Hou Duan Fa Yu Bu Liang , Chang Ran Se Ti Yin Xing
Name En
Craniometaphyseal Dysplasia, 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
Craniometaphyseal Dysplasia, Autosomal Recessive
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Umls
C2931244
Sym Map
SMDE03376
Etcm Disease
Craniometaphyseal Dysplasia, Autosomal Recessive
Itcmdb Generated
ITX-DISEASE-AA6D7EBA6A5B

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Page Title
Disease Craniometaphyseal Dysplasia, Autosomal Recessive Details page
Basic Information
Disease Name
Craniometaphyseal Dysplasia, Autosomal Recessive
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Bone diseases;Neuronal diseases;Oral diseases