Choroideremia

rare

Choroideremia (CHM) is an X-linked chorioretinal dystrophy characterized by progressive degeneration of the choroid, retinal pigment epithelium (RPE) and retina.

Identifiers: MONDO:0010557 OMIM:303100 Orphanet:180
Causal genes: CHM
Part of: X-linked disease Inherited retinal dystrophy Neurovascular disorder Optic choroid disorder
Also known as: CHM · progressive choroidal atrophy · progressive tapetochoroidal dystrophy · Tapetochoroidal dystrophy · TCD

Subtypes

All diseases Rare only

Disease	ID	Subtypes
Choroideremia hypopituitarism	MONDO:0022737
Total central choroidal atrophy	MONDO:0004889

Rare disease

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