Lymphatic Malformation 7 (LMPHM7)

Lymphatic Malformation 7(来自ICD-11)

别称:

Central Conduction Lymphatic Anomaly

Lmphm7

Hfasd

Ephb4-Related Generalized Lymphatic Dysplasia with Non-Immune Hydrops Fetalis

Ephb4-Related Generalized Lymphatic Dysplasia with Atrial Septal Defect

Hydrops Fetalis, Non-Immune, and/or Atrial Septal Defect

Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect

Ephb4-Related Lymphatic-Related Hydrops Fetalis

Lymphatic Malformation, Type 7

Ephb4-Related Lrhf/gld

Hydrops Fetalis

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Lymphatic Malformation 7, also known as central conduction lymphatic anomaly, is related to lymphatic malformation 12 and lymphatic malformation 1, and has symptoms including edema and peau d'orange. An important gene associated with Lymphatic Malformation 7 is EPHB4 (EPH Receptor B4). The drugs Anti-Arrhythmia Agents and Chrysarobin have been mentioned in the context of this disorder. Affiliated tissues include skin and lung, and related phenotypes are lymphedema and pleural effusion

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