Details of Disease | DrugMAP

General Information of Disease (ID: DISBHSXC)

Disease Name	Lymphatic malformation 8
Synonyms	LYMPHATIC MALFORMATION 8; LMPHM8
Disease Hierarchy	DIS4D8VL: Lymphatic malformation DISBHSXC: Lymphatic malformation 8
Disease Identifiers	MONDO ID MONDO_0032907 UMLS CUI C5231496 OMIM ID 618773 MedGen ID 1684767

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
CALCRL	TT67OLB	Limited	Unknown	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
CALCRL	OTMGGM47	Limited	Unknown	[1]
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References

1	hCALCRL mutation causes autosomal recessive nonimmune hydrops fetalis with lymphatic dysplasia. J Exp Med. 2018 Sep 3;215(9):2339-2353. doi: 10.1084/jem.20180528. Epub 2018 Aug 16.