Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome

rare

Identifiers: MONDO:0018681 Orphanet:453499
Part of: Congenital nervous system disorder Dysostosis Multiple congenital anomalies/dysmorphic syndrome-intellectual disability Neurodevelopmental disorder

Subtypes

Disease	ID	Subtypes	Genes
Au-Kline syndrome	MONDO:0014700		HNRNPK
Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome due to 9q21 microdeletion	MONDO:0018131

Rare disease

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