Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Formula: 17Herb: 12Symptom: 1Target: 18Links: 54
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 15249
- Core Entity Id
- 73157
- Source Entity Count
- 1
- Preferred Name
- Deafness, Autosomal Dominant 39, With Dentinogenesis Imperfecta 1
- Name Cn
- 常染色体显性遗传性耳聋39型伴牙本质发育不全1型
- Name Pinyin
- Chang Ran Se Ti Xian Xing Yi Chuan Xing Er Long 39 Xing Ban Ya Ben Zhi Fa Yu Bu Quan 1 Xing
- Name En
- Deafness, Autosomal Dominant 39, With Dentinogenesis Imperfecta 1
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Stomatognathic Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms; Otorhinolaryngologic Diseases
- Do Class
- Hpo Class
- Mesh Class Name
- Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases
- 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
Deafness, Autosomal Dominant 39, With Dentinogenesis Imperfecta 1
Role
preferred
Name
DFNA39/DENTINOGENESIS IMPERFECTA 1 SYNDROME
Role
alias
Name
DFNA39/DGI1 SYNDROME
Role
alias
Name
DGI1/DFNA39 SYNDROME
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS017014
Omim
605594
Umls
C1854146
Sym Map
SMDE03878
Dis Ge Net
C1854146
Umls Sty
T047
Me Sh Class
C07C09C10C16C23
Etcm Disease
Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1
Tcmbank Disease
18105
Itcmdb Generated
ITX-DISEASE-EEE21034B164
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Page Title
Disease Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1 Details page
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1
Global Category
Genetic diseases
Anatomical Category
Ear diseases
Me Sh Disease Class
Stomatognathic Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms; Otorhinolaryngologic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases
Umls Semantic Type Name
Disease or Syndrome