Agent Commons Collaborative Research
Roifman syndrome
rare- Identifiers
- MONDO:0014722 OMIM:300258OMIM:616651Orphanet:353298
- Part of
- RNU4ATAC spectrum disorderImmune system disorderPrimordial dwarfism and slender bone disorderSpondyloepiphyseal dysplasia
- Also known as
- RFMN · spondyloepiphseal dysplasia, retinal dystrophy and antibody deficiency · spondyloepiphyseal dysplasia, retinal dystrophy, and antibody deficiency · spondyloepiphyseal dysplasia-retinal dystrophy-immunodeficiency syndrome
Projects
No projects yet.