DiseaseID 26136

先天性非甲状腺肿性甲状腺功能减退症5型

Hypothyroidism, Congenital, Nongoitrous, 5

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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: 1Target: 18Links: 24
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
26136
Core Entity Id
118704
Source Entity Count
1
Preferred Name
Hypothyroidism, Congenital, Nongoitrous, 5
Name Cn
先天性非甲状腺肿性甲状腺功能减退症5型
Name Pinyin
Xian Tian Xing Fei Jia Zhuang Xian Zhong Xing Jia Zhuang Xian Gong Neng Jian Tui Zheng 5 Xing
Name En
Hypothyroidism, Congenital, Nongoitrous, 5
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
Suppressed
No

Names

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

Name
Hypothyroidism, Congenital, Nongoitrous, 5
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Umls
C2673630
Sym Map
SMDE02079
Etcm Disease
Hypothyroidism, Congenital, Nongoitrous, 5
Itcmdb Generated
ITX-DISEASE-83FD6D76A53D

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0
Page Title
Disease Hypothyroidism, Congenital, Nongoitrous, 5 Details page
Basic Information
Disease Name
Hypothyroidism, Congenital, Nongoitrous, 5
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Bone diseases;Endocrine diseases;Neuronal diseases