2p21 microdeletion syndrome

MONDO:0015583

The 2p21 microdeletion syndrome consists of cystinuria, neonatal seizures, hypotonia, severe growth and developmental delay, facial dysmorphism, and lactic acidemia.

Also known as: 2p21 deletion syndrome, 2p21 microdeletion syndrome, Del(2)(p21), monosomy 2p21

0 clinical trials for this condition and its sub-types, 0 tagged with 2p21 microdeletion syndrome itself.

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Part of

↑ Partial deletion of the short arm of chromosome 2 (0)

Sub-types of 2p21 microdeletion syndrome

2p21 microdeletion syndrome without cystinuria 0 trials

Including sub-types (0) Tagged with 2p21 microdeletion syndrome (0)

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