Hypomyelinating leukodystrophy 10

MONDO:0014632

Any leukodystrophy in which the cause of the disease is a mutation in the PYCR2 gene.

Also known as: HLD10, PYCR2 leukodystrophy, PYCR2-related microcephaly-progressive leukoencephalopathy, hypomyelinating leukodystrophy type 10, leukodystrophy caused by mutation in PYCR2, leukodystrophy, hypomyelinating, 10, leukodystrophy, hypomyelinating, type 10

0 clinical trials for this condition and its sub-types, 0 tagged with Hypomyelinating leukodystrophy 10 itself.

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↑ Congenital nervous system disorder (284) ↑ Leukodystrophy (72) ↑ Multiple congenital anomalies/dysmorphic syndrome-intellectual disability (59)

Including sub-types (0) Tagged with Hypomyelinating leukodystrophy 10 (0)

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