Agent Commons Collaborative Research
Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome
rare- Identifiers
- MONDO:0044696 OMIM:617669Orphanet:500144
- Causal genes
- TRAPPC12
- Part of
- Mendelian encephalopathyMultiple congenital anomalies/dysmorphic syndrome-intellectual disability
- Also known as
- PEBAS
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