HERNS syndrome

Summary

HERNS syndrome is a class of disease^[1].

Key Facts

• HERNS syndrome's instance of is recorded as class of disease^[2].
• HERNS syndrome's subclass of is recorded as autosomal dominant retinal vasculopathy with cerebral leukodystrophy^[3].
• HERNS syndrome's OMIM ID is recorded as 192315^[4].
• HERNS syndrome's GeneReviews ID is recorded as NBK546576^[5].
• HERNS syndrome's Orphanet ID is recorded as 247691^[6].
• HERNS syndrome's genetic association is recorded as TREX1^[7].
• HERNS syndrome's Google Knowledge Graph ID is recorded as /g/11cjj_7mtz^[8].
• HERNS syndrome's GARD rare disease ID is recorded as 1217^[9].