GATA2 - 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
GATA2 Deficiency	causative germline	mechanism: GATA2 Haploinsufficiency subtype: MonoMAC
deafness-lymphedema-leukemia syndrome	untyped Causal heterozygous loss-of-function variant	mechanism: GATA2 haploinsufficiency

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
GATA2 deficiency with susceptibility to MDS/AML MONDO:0042982	AD	Definitive 2022-12-30	GATA2 Deficiency causative

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