Developmental delay with short stature, dysmorphic facial features, and sparse hair 1

Any developmental delay with short stature, dysmorphic facial features, and sparse hair in which the cause of the disease is a mutation in the DPH1 gene.

Also known as: developmental delay with short stature, dysmorphic facial features, and sparse hair, developmental delay-short stature-dysmorphic features-sparse hair syndrome, DEDSSH1, developmental delay with short stature, dysmorphic features, and sparse hair 1, diphtamide deficiency syndrome, Loucks-Innes syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with Developmental delay with short stature, dysmorphic facial features, and sparse hair 1 itself.