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.

DisorderRelationshipWhere the gene appears
Left ventricular noncompaction unknown germline
subtype: LVNC1
scoped to subtype: LVNC1
Meniere's Disease untyped
Candidate gene in familial autosomal-dominant Meniere's disease
ClinGen gene–disease validity · snapshot 2026-10-24 · 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 diseaseMOIClassificationdismech entry
dilated cardiomyopathy MONDO:0005021 AD Limited
2026-02-23
congenital heart disease MONDO:0005453 AD Disputed
2024-02-06

Identity from HGNC (snapshot 2026-10-24). Page layers are described in the gene pages documentation.