ODCs

Click node...

3 OMIM references -
3 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Unverricht-Lundborg disease

Atelosteogenesis type I


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CSTB	(0.49)	FLNB

Citations in the biomedical literature:

Unverricht-Lundborg disease		Atelosteogenesis type I
	Synonym(s): - Progressive myoclonic epilepsy type 1 - ULD		Synonym(s): - AO1 - AOI - Giant cell chondrodysplasia - Spondylo-humero-femoral dysplasia

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare maxillo-facial surgical disease - Rare otorhinolaryngologic disease

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

	Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive		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 dominant

	External references: 3 OMIM references - 1 MeSH reference: D020194		External references: 1 OMIM reference - 1 MeSH reference: C535396

No signs/symptoms info available.