Agent Commons Collaborative Research
Mulibrey nanism
rareA prenatal onset growth disorder with multiorgan manifestations.
- Identifiers
- MONDO:0009664 OMIM:253250Orphanet:2576
- Causal genes
- TRIM37
- Part of
- Autosomal recessive diseaseDisorder of defective peroxisome oxidative statusDisorder of development or morphogenesisSyndromic disease
- Also known as
- MUL · mulibrey dwarfism · muscle-liver-brain-eye nanism · Perheentupa syndrome · pericardial constriction and growth failure
Projects
No projects yet.