DiseaseID 18308

线状皮肤缺损伴多发性先天畸形2型

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: 2Target: 17Links: 26
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Record Fields

Scalar fields from the final disease record.

Disease Id
18308
Core Entity Id
76686
Source Entity Count
1
Preferred Name
Linear Skin Defects With Multiple Congenital Anomalies 2
Name Cn
线状皮肤缺损伴多发性先天畸形2型
Name Pinyin
Xian Zhuang Pi Fu Que Sun Ban Duo Fa Xing Xian Tian Ji Xing 2 Xing
Name En
Linear Skin Defects With Multiple Congenital Anomalies 2
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Do Class
Hpo Class
Mesh Class Name
Hpo Class Name
Do Class Name
Disease Definition
Version
v1
Suppressed
No

Names

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

Name
Linear Skin Defects With Multiple Congenital Anomalies 2
Role
preferred
Name
APLASIA CUTIS CONGENITA, RETICULOLINEAR, WITH MICROCEPHALY, FACIAL DYSMORPHISM, AND OTHER CONGENITAL ANOMALIES
Role
alias
Name
APLCC
Role
alias
Name
LSDMCA2
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS021708
Omim
300887
Umls
C3550921
Sym Map
SMDE01904
Dis Ge Net
C3550921
Umls Sty
T047
Etcm Disease
Linear Skin Defects with Multiple Congenital Anomalies 2
Tcmbank Disease
564
Itcmdb Generated
ITX-DISEASE-76C63A45F4CC

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0
Page Title
Disease Linear Skin Defects with Multiple Congenital Anomalies 2 Details page
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Linear Skin Defects with Multiple Congenital Anomalies 2
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Cardiovascular diseases;Eye diseases;Neuronal diseases;Skin diseases
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome