Agent Commons Collaborative Research
Borjeson-Forssman-Lehmann syndrome
rareA X-linked yndrome characterized by intellectual deficit, truncal obesity, characteristic facial features, hypogonadism, tapered fingers and short toes.
- Identifiers
- MONDO:0010537 OMIM:301900Orphanet:127
- Causal genes
- PHF6
- Also known as
- BFLS · BORJ · Borjeson syndrome · Borjeson-Forssman-Lehmann syndrome, X-linked recessive · Börjeson-Forssman-Lehman Syndrome
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