Clinical Indication ID & Name
R85
Holoprosencephaly - NOT chromosomal
Test Group
Neurology
Specialties
Test code
R85.2
Test name
N/A
Target genes
Holoprosencephaly (78)
Test scope
n/a
Test method/ technology
WGS
Optimal Family Structure
n/a
Eligibility Criteria
Liveborn individuals with unexplained holoprosencephaly in whom a chromosomal cause has been excluded by microarray or equivalent
Commissioning group
Specialised
Overlapping idications
n/a
Address for samples/request forms
North Thames GLH, Rare & Inherited Disease Genomic Laboratory
Specimen Reception, Level 5 Barclay House, 37 Queen Square,
London WC1N 3BH
Contact with queries
Supporting documents
Rare Disese WGS Clinician pack
Education resources
n/a
Service updates
n/a
Request form download
Consent record
See consent guidance in test request form
Sample requirements
See sample guidance in test request form