Category:Börjeson-Forssman-Lehmann syndrome

**Borjeson-Forssman-Lehmann syndrome**
	genetic condition in humans
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Instance of	developmental defect during embryogenesis; rare disease; class of disease;
Subclass of	X-linked intellectual disability; syndromic obesity; multiple congenital anomalies/dysmorphic syndrome-intellectual disability; ptosis; X-linked recessive disease;
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	Q1019940;
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