Hypotonia, ataxia, and delayed development syndrome

MONDO:0015021

Also known as: EBF3 neurodevelopmental disorder, HADDS, developmental delay-ataxia-hypotonia-facial dysmorphism syndrome, hypotonia, ataxia, and delayed development syndrome, hypotonia, ataxia, and delayed development syndrome; HADDS

0 clinical trials for this condition and its sub-types, 0 tagged with Hypotonia, ataxia, and delayed development syndrome itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Hereditary disease (18187) ↑ Multiple congenital anomalies/dysmorphic syndrome-intellectual disability (59)

Including sub-types (0) Tagged with Hypotonia, ataxia, and delayed development syndrome (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.