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Lattice corneal dystrophy type I

2 OMIM references -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
4 associated genes
8 signs/symptoms

Lattice corneal dystrophy type I

Schizencephaly

TGFBI	(UniProt - OMIM)		COL4A1	(UniProt - OMIM)
			EMX2	(UniProt - OMIM)
			SHH	(UniProt - OMIM)
			SIX3	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TGFBI	(0.52)	COL4A1

Citations in the biomedical literature:

Lattice corneal dystrophy type I		Schizencephaly
	Synonym(s): - Biber-Haab-Dimmer dystrophy - Classic lattice corneal dystrophy - LCD1 - LCDI - Lattice corneal dystrophy type 1		Synonym(s): (no synonyms)

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

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

	Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

	External references: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

Schizencephaly
	Very frequent - Corpus callosum / septum pellucidum total / partial agenesis - EEG anomalies - Hypertonia / spasticity / rigidity / stiffness - Porencephaly - Strabismus / squint Frequent - Hemiplegia / diplegia / hemiparesia / limb palsy - Intellectual deficit / mental / psychomotor retardation / learning disability - Seizures / epilepsy / absences / spasms / status epilepticus
Lattice corneal dystrophy type I
(no data available)