Details of Disease | DrugMAP

General Information of Disease (ID: DISJ0LQ0)

Disease Name	Erythrocytosis, familial, 7
Synonyms	erythrocytosis, Alpha-globin type; erythrocytosis, FAMILIAL, 7; polycythemia, Alpha-globin type; ECYT7; erythrocytosis 7
Disease Hierarchy	DISOIGHH: Familial polycythemia DISJ0LQ0: Erythrocytosis, familial, 7
Disease Identifiers	MONDO ID MONDO_0054802 UMLS CUI C4693823 OMIM ID 617981 MedGen ID 1642594

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
HBA2	TTQO71U	Strong	Autosomal dominant	[1]
------------------------------------------------------------------------------------

This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
HBA2	OTW2BQF4	Strong	Autosomal dominant	[1]
------------------------------------------------------------------------------------

References

1	The Gene Curation Coalition: A global effort to harmonize gene-disease evidence resources. Genet Med. 2022 Aug;24(8):1732-1742. doi: 10.1016/j.gim.2022.04.017. Epub 2022 May 4.