lymphatic malformation 2
Also known as: LMPH1B, lymphedema, hereditary, 1B
Also known as: LMPH1B, lymphedema, hereditary, 1B
Also known as: GJC2 hereditary lymphedema, LMPH1C, hereditary lymphedema caused by mutation in GJC2, lymphedema, hereditary, 1C, lymphedema, hereditary, IC, lymphedema, hereditary, type 1C
Also known as: LMPH1D, VEGFC hereditary lymphedema, hereditary lymphedema caused by mutation in VEGFC, lymphedema, hereditary, 1D, lymphedema, hereditary, type 1D
Also known as: LMPH2, Meige disease, Meige lymphedema, hereditary lymphedema type II, late-onset lymphedema, late-onset primary lymphedema, lymphedema hereditary type 2, lymphedema praecox, lymphedema preacox, lymphedema, hereditary, II, lymphedema, late-onset
Also known as: LMPH3, generalised lymphatic dysplasia of Fotiou, generalized lymphatic dysplasia of Fotiou, lymphedema, hereditary, 3, lymphedema, hereditary, III, lymphedema, hereditary, type III
Also known as: HFASD, hydrops fetalis, nonimmune, and/or atrial septal defect, susceptibility to, hydrops fetalis, nonimmune, and/or atrial septal defect, susceptibility to; HFASD
Also known as: LMPHM8, LYMPHATIC MALFORMATION 8
Also known as: LMPHM9, lymphatic malformation 9
Also known as: Irons Bhan syndrome, Irons-Bhan syndrome, Irons-Bianchi syndrome, autosomal recessive syndrome of lymphedema, hydroceles, atrial septal defect, and characteristic facial changes, lymphedema, CARDIAC septal defects, and characteristic facies, lymphedema, atrial septal defect, and characteristic facial changes, lymphedema, atrial septal defect, and characteristic facies
Please complete this form to access the requested resource.