DiseaseID 29797
莫尔-克劳森综合征
Mohr-Claussen Syndrome
JABL99:A syndrome consisting mainly of orofacial and digital defects, including microcephaly, lingual defects, median cleft of the upper lip, and bony changes of the hands and feet. Psychomotor retardation has been repor
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Disease: 1Symptom: 6Target: 8Links: 14
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 29797
- Core Entity Id
- 122365
- Source Entity Count
- 1
- Preferred Name
- Mohr-Claussen Syndrome
- Name Cn
- 莫尔-克劳森综合征
- Name Pinyin
- Mo Er - Ke Lao Sen Zong He Zheng
- Name En
- Mohr-Claussen Syndrome
- 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:A syndrome consisting mainly of orofacial and digital defects, including microcephaly, lingual defects, median cleft of the upper lip, and bony changes of the hands and feet. Psychomotor retardation has been reported in some cases.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Mohr-Claussen Syndrome
Role
preferred
Source
SymMap_v2
Preferred
Yes
Cross References
Trusted external identifiers retained for this final record.
Umls
C0026363
Sym Map
SMDE11065
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Definition
JABL99:A syndrome consisting mainly of orofacial and digital defects, including microcephaly, lingual defects, median cleft of the upper lip, and bony changes of the hands and feet. Psychomotor retardation has been reported in some cases.