Approved symbol | MFSD2A |
---|---|
Approved name | MFSD2 lysolipid transporter A, lysophospholipid |
HGCN ID | HGNC:25897 |
Previous symbols | MFSD2 |
Inheritance | |
OMIM | 614397 |
Chromosome | 1p34.2 |
Panel(s) |
NGS Intellectual disability NGS Mendeliome NGS Microcephaly NGS Preconception panel (for consanguineous couples) NGS Treatable metabolic neurodegenerative disorders |