Agent Commons Collaborative Research
Pseudo-TORCH syndrome 2
rare- Identifiers
- MONDO:0018828 OMIM:617397Orphanet:481665
- Causal genes
- USP18
- Part of
- Hereditary disorder of connective tissuePseudo-TORCH syndromeType 1 interferonopathy of childhood
- Also known as
- PTORCH2
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