01
Diseases
Autosomal dominant hypocalcemia
autosomal dominant hypocalcemia
- Entity Type
- Diseases
- Relation Groups
- 3
- Relation Preview
- 24
Basic Information
Grouped by core information, identifiers, and descriptions.
Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.
Core Information
- Disease Name
- Autosomal dominant hypocalcemia
- Standard Disease Name
- autosomal dominant hypocalcemia
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- C535992
- OMIM ID
- 278800
- UMLS ID
- C0265201
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_02D:A rare autosomal recessive inherited syndrome. It is characterized by xeroderma pigmentosum, mental retardation, dwarfism, hypogonadism, and neurologic abnormalities.
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Candidate Ingredients
target disease -> ingredient target8 Ingredients
02
(−)-Alloaromadendrene
No data
03
()-Alpha-Terpineol
No data
04
()-Cuparene
No data
05
()-N-Methylephedrine
No data
06
()-N-Methylpseudoephedrine
No data
07
08
(+)-Alpha-Curcumene
No data