GenTIGS

List of monogenic disorders and their associated genes
Monogenic disorders arise from mutations in a single gene, but variations within that gene or in multiple genes can also lead to similar phenotypes, typically following Mendelian inheritance patterns associated with specific genetic changes.

View information by inheritance mode

S.No.	Genetic Disorders Modes of inheritance	Category	Gene symbol	Indian context	Links
411	von Willebrand disease Autosomal dominant, Autosomal recessive	Blood disorders	VWF von Willebrand factor	Reports Updated as of Nov 30, 2023	PubMed
412	Waldenstrom macroglobulinemia	Cancer disorders	MYD88 MYD88 innate immune signal transduction adaptor	Reports Updated as of Feb 20, 2024	PubMed
413	Werner syndrome Autosomal recessive	Aging disorders	WRN WRN RecQ like helicase	Reports Updated as of Feb 01, 2025	PubMed
414	Williams syndrome Autosomal dominant	Neurodevelopmental disorders	ELN elastin	Reports Updated as of Sep 05, 2023	PubMed
415	Wilson disease Autosomal recessive	Metabolic disorders	ATP7B ATPase copper transporting beta	Reports Updated as of Sep 05, 2023	PubMed
416	Winchester syndrome Autosomal recessive	Bone disorders	MMP14 matrix metallopeptidase 14	Reports Updated as of Sep 05, 2023	PubMed
417	Wolcott-Rallison dysplasia Autosomal recessive	Multisystemic disorders	EIF2AK3 eukaryotic translation initiation factor 2 alpha kinase 3	Reports Updated as of Feb 01, 2025	PubMed
418	Wolman disease Autosomal recessive	Metabolic disorders	LIPA lipase A, lysosomal acid type	Reports Updated as of Nov 02, 2023	PubMed
419	X-linked agammaglobulinemia X-linked dominant	Immune disorders	BTK Bruton tyrosine kinase	Reports Updated as of Jul 20, 2024	PubMed
420	X-linked myopathy with excessive autophagy X-linked recessive	Neuromuscular disorders	VMA21 vacuolar ATPase assembly factor VMA21	Reports Updated as of Feb 01, 2025	PubMed

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