ODCs

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

PROTEIN INTERACTIONS: 2

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

Thiel-Behnke corneal dystrophy

Autosomal dominant Alport syndrome

TGFBI	(UniProt - OMIM)		COL4A3	(UniProt - OMIM)
			COL4A4	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TGFBI TGFBI	(0.52) (0.52)	COL4A3 COL4A4

Citations in the biomedical literature:

Thiel-Behnke corneal dystrophy		Autosomal dominant Alport syndrome
	Synonym(s): - Anterior limiting membrane dystrophy type II - Corneal dystrophy of Bowman layer type II - Curly fiber corneal dystrophy - Honeycomb corneal dystrophy - TBCD - Waardenburg-Jonker corneal dystrophy		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare eye disease - Rare genetic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease - Rare otorhinolaryngologic disease - Rare renal 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: adolescence / young Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: - Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C536586

No signs/symptoms info available.