01
ROGDI
No data
Diseases
Amelocerebrohypohidrotic Syndrome
amelocerebrohypohidrotic syndrome
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 1
Basic Information
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Core Information
- Disease Name
- Amelocerebrohypohidrotic Syndrome
- Standard Disease Name
- amelocerebrohypohidrotic syndrome
- MeSH Tree
- No data
- ICD-10
- G40.8
Identifiers
- DO ID
- No data
- MeSH ID
- C537213
- OMIM ID
- 226750
- UMLS ID
- C0406740
- HPO ID
- No data
Description and Extensions
- Description
- Kohlschütter-T？nz syndrome (KTS) is a genetically heterogeneous autosomal recessive syndrome characterized by the triad of amelogenesis imperfect, infantile onset epilepsy, intellectual disability wit
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Related Targets
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