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Amyotrophic lateral sclerosis-parkinsonism-dementia complex
1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Primary hypomagnesemia with secondary hypocalcemia
1 OMIM reference -
1 associated gene
No signs/symptoms info
Amyotrophic lateral sclerosis-parkinsonism-dementia complex
Primary hypomagnesemia with secondary hypocalcemia

PARK7
(UniProt - OMIM)
 TRPM6
(UniProt - OMIM)
TRPM7
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
TRPM7
(0.55)
TRPM6


Citations in the biomedical literature:


Amyotrophic lateral sclerosis-parkinsonism-dementia complex
PARK7 TRPM7
Primary hypomagnesemia with secondary hypocalcemia
TRPM6



Amyotrophic lateral sclerosis-parkinsonism-dementia complex
Primary hypomagnesemia with secondary hypocalcemia

Synonym(s):
- Amyotrophic lateral sclerosis-parkinsonism-dementia of Guam
- Guam disease
- Lytico-Bodig disease
- PDALS
- Parkinsonism-dementia-ALS complex
Synonym(s):
- HOMG1
- HSH
- Hypomagnesemia caused by selective magnesium malabsorption
- Hypomagnesemia intestinal type 1
- Intestinal hypomagnesemia with secondary hypocalcemia
- PHSH
Classification (Orphanet):
- Rare neurologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: before age 5
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.