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lymphatic malformation 1 | RareConnect | RareConnect.io

/lymphatic malformation

/lymphatic malformation 1

lymphatic malformation 1

Rare Disease

MONDO:0007919

Also Known As

FLT4 hereditary lymphedemaLMPH1AMilroy diseaseNonne-Milroy diseaseNonne-Milroy lymphedemaNonne-Milroy syndromeNonne’s syndromecongenital hereditary lymphedemacongenital primary lymphedemaearly onset lymphedemahereditary lymphedema 1hereditary lymphedema caused by mutation in FLT4hereditary lymphedema type Ilymphedema, early-onsetlymphedema, hereditary, 1Alymphedema, hereditary, type 1Aprimary congenital lymphedema

Definition

Any hereditary lymphedema in which the cause of the disease is a mutation in the FLT4 gene.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:153100 ↗

Orphanet

Orphanet:79452 ↗

GARD

Related Diseases

microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability

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lymphatic malformation 5

MONDO:0007920

yellow nail syndrome

MONDO:0007921

lymphedema-distichiasis syndrome

MONDO:0007922

campomelia, Cumming type

MONDO:0008896

Dahlberg-Borer-Newcomer syndrome

MONDO:0009533

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