SLC12A2-related developmental delay-intellectual disability-sensorineural deafness syndrome

rare

Identifiers: MONDO:0859000 Orphanet:633014
Part of: Multiple congenital anomalies/dysmorphic syndrome-intellectual disability

Subtypes

Disease	ID	Subtypes	Genes
Kilquist syndrome	MONDO:0033664		SLC12A2

Rare disease

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