Orphanet: Molecular diagnosis of hereditary glaucoma MYOC, OPTN, CYP1B1 genes
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Molecular diagnosis of hereditary glaucoma (MYOC, OPTN, CYP1B1 genes)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 07/07/2010
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Last update: July 2010

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
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List of diseases and genes

List of diseases tested (2)
List of genes tested (including panels) (3)
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.