Agent Commons Collaborative Research
Mucopolysaccharidosis-plus syndrome
rare- Identifiers
- MONDO:0015012 OMIM:617303Orphanet:505248
- Causal genes
- VPS33A
- Part of
- Developmental anomaly of metabolic originLysosomal storage disease with skeletal involvementMucopolysaccharidosis or mucopolysaccharidosis-like disorderMultiple congenital anomalies/dysmorphic syndrome-intellectual disabilityRespiratory system disorder
- Also known as
- MPSPS · mucopolysaccharidosis-like plus disease · mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders
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