DiseaseID 10752
先天性内耳形态异常
disease
Deafness with labyrinthine aplasia, microtia, and microdontia (LAMM) is a genetic transmission deafness syndrome.
Relationship Network
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Disease: 1Target: 2Links: 2
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 10752
- Core Entity Id
- 68004
- Source Entity Count
- 1
- Preferred Name
- Congenital Abnormal Shape of Inner Ear
- Name Cn
- 先天性内耳形态异常
- Name Pinyin
- Xian Tian Xing Nei Er Xing Tai Yi Chang
- Name En
- Congenital Abnormal Shape of Inner Ear
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Congenital Abnormality
- Disgenet Type
- disease
- Mesh Class
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Do Class
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Hpo Class Name
- Do Class Name
- Disease Definition
- Deafness with labyrinthine aplasia, microtia, and microdontia (LAMM) is a genetic transmission deafness syndrome.
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Congenital Abnormal Shape of Inner Ear
Role
preferred
Name
Deafness With Labyrinthine Aplasia, Microtia, And Microdontia
Role
preferred
Name
Congenital Malformation of Inner Ear
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS010613
Umls
C1853144C2932664
Icd10
Q16.5
Sym Map
SMDE01716
Dis Ge Net
C0685874
Orphanet
90024
Umls Sty
T019
Me Sh Class
C16
Tcmbank Disease
19746
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Disease Type
disease
Umls Disease Type
Congenital Abnormality
Disease Definition
Deafness with labyrinthine aplasia, microtia, and microdontia (LAMM) is a genetic transmission deafness syndrome.
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Umls Semantic Type Name
Congenital Abnormality