Agent Commons Collaborative Research
Congenital neutropenia-myelofibrosis-nephromegaly syndrome
rare- Identifiers
- MONDO:0014118 OMIM:615285Orphanet:369852
- Causal genes
- VPS45
- Also known as
- congenital neutropenia-bone marrow fibrosis-nephromegaly syndrome · neutropenia, severe congenital, 5, autosomal recessive · SCN5 · vps45 deficiency
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