Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Formula: 17Symptom: 3Target: 16Links: 44
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 15300
- Core Entity Id
- 73216
- Source Entity Count
- 1
- Preferred Name
- Molybdenum Cofactor Deficiency, Complementation Group B
- Name Cn
- 钼辅因子缺乏症，互补组B
- Name Pinyin
- Mu Fu Yin Zi Que Fa Zheng ， Hu Bu Zu B
- Name En
- Molybdenum Cofactor Deficiency, Complementation Group B
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
- Do Class
- genetic disease; disease of metabolism
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
- Hpo Class Name
- Do Class Name
- disease of metabolism; genetic disease
- Disease Definition
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Molybdenum Cofactor Deficiency, Complementation Group B
Role
preferred
Name
MOCODB
Role
alias
Name
Molybdenum Cofactor Deficiency Type B
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS017091
Omim
252160
Umls
C1854989
Sym Map
SMDE00294
Do Class
DOID:0014667DOID:630
Dis Ge Net
C1854989
Umls Sty
T047
Me Sh Class
C16C18
Etcm Disease
Molybdenum Cofactor Deficiency, Complementation Group B
Tcmbank Disease
17419
Itcmdb Generated
ITX-DISEASE-8CF7C1841093
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease Molybdenum Cofactor Deficiency, Complementation Group B Details page
Do Class Name
disease of metabolism; genetic disease
Disease Type
disease
Do Disease Class
genetic disease; disease of metabolism
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Molybdenum Cofactor Deficiency, Complementation Group B
Global Category
Fetal diseases;Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Eye diseases;Nephrological diseases;Neuronal diseases
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Umls Semantic Type Name
Disease or Syndrome