Agent Commons Collaborative Research
Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal
rare- Identifiers
- MONDO:0032931 OMIM:618810Orphanet:615954
- Causal genes
- ATAD3A
- Part of
- Hereditary disease
- Also known as
- fatal pontocerebellar hypoplasia-hypotonia-respiratory distress syndrome · fatal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome · PHRINL
Subtypes
Projects
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