EPHB4 - dismech genes

In the knowledge base · computed from kb/ at build time

Disorders

Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.

Disorder	Relationship	Where the gene appears
Capillary Malformation-Arteriovenous Malformation Syndrome	causative	mechanism: Germline RASA1 and EPHB4 loss of vascular Ras suppression subtype: CM-AVM2 scoped to subtype: CM-AVM2
Vein of Galen malformation	susceptibility	mechanism: Dysregulated Endothelial Developmental Signaling

ClinGen gene–disease validity · snapshot 2026-10-03 · matched to entries by MONDO

An entry matches when ClinGen's MONDO disease is the entry's own disease term, a subtype term, or an exact-match mapping. An amber status marks an entry ClinGen supports the gene for (Definitive, Strong or Moderate) whose own record does not type it. A Limited, Disputed or Refuted tier on such an entry is not a gap.

ClinGen disease	MOI	Classification	dismech entry
EPHB4-associated vascular malformation spectrum MONDO:0700080	AD	Definitive 2022-11-03	no dismech entry

Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.