DiseaseID 29718
X连锁智力障碍16型
Mental Retardation, X Linked 16
JABL99:Nonsyndromic mental retardation. Variable minor clinical features include hypotonia, microcephaly, hypoactivity, feeding difficulty, intrauterine growth retardation, visual impairment, and seizures.
Relationship Network
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Disease: 1Symptom: 4Target: 7Links: 11
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 29718
- Core Entity Id
- 122286
- Source Entity Count
- 1
- Preferred Name
- Mental Retardation, X Linked 16
- Name Cn
- X连锁智力障碍16型
- Name Pinyin
- X Lian Suo Zhi Li Zhang Ai 16 Xing
- Name En
- Mental Retardation, X Linked 16
- 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
- JABL99:Nonsyndromic mental retardation. Variable minor clinical features include hypotonia, microcephaly, hypoactivity, feeding difficulty, intrauterine growth retardation, visual impairment, and seizures.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Mental Retardation, X Linked 16
Role
preferred
Source
SymMap_v2
Preferred
Yes
Cross References
Trusted external identifiers retained for this final record.
Sym Map
SMDE10889
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Definition
JABL99:Nonsyndromic mental retardation. Variable minor clinical features include hypotonia, microcephaly, hypoactivity, feeding difficulty, intrauterine growth retardation, visual impairment, and seizures.