Developmental delay with short stature, dysmorphic facial features, and sparse hair 2

MONDO:0100217

Any developmental delay with short stature, dysmorphic facial features, and sparse hair in which the cause of the disease is a mutation in the DPH2 gene.

Also known as: DEDSSH2, diphthamide deficiency syndrome 2

0 clinical trials for this condition and its sub-types, 0 tagged with Developmental delay with short stature, dysmorphic facial features, and sparse hair 2 itself.

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