ODCs

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1 OMIM reference -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
2 associated genes
No signs/symptoms info

Amyotrophic lateral sclerosis-parkinsonism-dementia complex

Familial ocular anterior segment mesenchymal dysgenesis

PARK7	(UniProt - OMIM)		FOXE3	(UniProt - OMIM)
TRPM7	(UniProt - OMIM)		PITX3	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PARK7	(0.52)	PITX3

Citations in the biomedical literature:

Amyotrophic lateral sclerosis-parkinsonism-dementia complex		Familial ocular anterior segment mesenchymal dysgenesis
	Synonym(s): - Amyotrophic lateral sclerosis-parkinsonism-dementia of Guam - Guam disease - Lytico-Bodig disease - PDALS - Parkinsonism-dementia-ALS complex		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare neurologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.