Lymphatic Malformation 1 (LMPHM1)

Lymphatic Malformation 1(来自ICD-11)

别称:

Milroy Disease

Hereditary Lymphedema Type I

Nonne-Milroy Lymphedema

Primary Congenital Lymphedema

Lymphedema, Hereditary, Type I, Formerly

Lymphedema, Hereditary, Ia, Formerly

Lymphedema, Early-Onset

Lmphm1

Pcl

Congenital Familial Lymphedema

Lymphatic Malformation, Type 1

Lymphedema Hereditary Type Ia

Lymphedema, Hereditary, 1a

Lymphedema Early-Onset

Lmph1a, Formerly

Milroy's Disease

Lmph1a

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Lymphatic Malformation 1, also known as milroy disease, is related to hereditary lymphedema i and hereditary lymphedema. An important gene associated with Lymphatic Malformation 1 is FLT4 (Fms Related Receptor Tyrosine Kinase 4), and among its related pathways/superpathways are Angiogenesis (CST) and Tyrosine Kinases / Adaptors. Affiliated tissues include skin and testis, and related phenotypes are lymphedema and hyperkeratosis

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