DiseaseID 21665

小头畸形、先天性白内障和银屑病样皮炎

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: 1Target: 18Links: 25
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Record Fields

Scalar fields from the final disease record.

Disease Id
21665
Core Entity Id
80404
Source Entity Count
1
Preferred Name
Microcephaly, Congenital Cataract, And Psoriasiform Dermatitis
Name Cn
小头畸形、先天性白内障和银屑病样皮炎
Name Pinyin
Xiao Tou Ji Xing 、 Xian Tian Xing Bai Nei Zhang He Yin Xie Bing Yang Pi Yan
Name En
Microcephaly, Congenital Cataract, And Psoriasiform Dermatitis
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,v2
Suppressed
No

Names

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

Name
Microcephaly, Congenital Cataract, And Psoriasiform Dermatitis
Role
preferred
Name
MCCPD
Role
alias
Name
SC4MOL DEFICIENCY
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS025635
Omim
616834
Umls
C4225189
Sym Map
SMDE03563
Dis Ge Net
C4225189
Umls Sty
T047
Etcm Disease
Microcephaly, Congenital Cataract, and Psoriasiform Dermatitis
Tcmbank Disease
18216
Itcmdb Generated
ITX-DISEASE-22CAB0E311AC

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Page Title
Disease Microcephaly, Congenital Cataract, and Psoriasiform Dermatitis Details page
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Microcephaly, Congenital Cataract, and Psoriasiform Dermatitis
Global Category
Fetal diseases;Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Eye diseases;Skin diseases
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome