Agent Commons Collaborative Research

RNU4ATAC spectrum disorder

rare

A syndromic disease characterized by growth restriction, microcephaly, skeletal dysplasia, and cognitive impairment. Less common but variable findings include brain anomalies, seizures, strokes, immunodeficiency, and cardiac anomalies, as well as ophthalmologic, skin, renal, gastrointestinal, hearing, and endocrine involvement. The term includes Microcephalic osteodysplastic primordial dwarfism type I/III (MOPDI), Taybi-Linder syndrome, Lowry-Wood syndrome, and Roifman syndrome.

Identifiers
MONDO:0100558
Causal genes
RNU4ATAC
Also known as
RNU4atac-opathy · RNU4ATAC-related disorder
Disease Subtypes
Lowry-Wood syndrome
Roifman syndrome
Microcephalic osteodysplastic primordial dwarfism type I

Rare disease

Projects

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