Disease #05780 (LMPHM (lymphatic malformation (LMPHM)))

Official abbreviation LMPHM
Name lymphatic malformation (LMPHM)
OMIM ID -
Inheritance -
Individuals reported having this disease 6
Phenotype entries for this disease 6
Associated with 1 gene ANGPT2
Associated tissues -
Disease features -
Remarks -
Date created 2020-07-09 16:12:34 +02:00 (CEST)
Date last edited N/A


Individuals

6 entries on 1 page. Showing entries 1 - 6.
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00305893 8 - - M - China - - - - - LMPHM - EPHB4 EPHB4 1 1 Sha Hong
00405725 LE-851-10 PubMed: Leppanen 2020 2-generation family, 1 affected, unaffected non-carrier parents M - Belgium - - - - - LMPHM see paper; ... ANGPT2 ANGPT2 1 1 Audrey Debue
00405726 LE-128-10 PubMed: Leppanen 2020 2-generation family, affected father/daughter F;M - Italy - - - - - LMPHM see paper; ... ANGPT2 ANGPT2 1 2 Audrey Debue
00405727 LE-65-10 PubMed: Leppanen 2020 2-generation family, affected son/carrier father M - Israel - - - - - LMPHM see paper; ... ANGPT2 ANGPT2 1 1 Audrey Debue
00405728 LE-148-1000 PubMed: Leppanen 2020 3-generation family, affected grandfather/father/son M - Italy - - - - - LMPHM see paper; ... ANGPT2 ANGPT2 1 3 Audrey Debue
00405729 LE-623-10 PubMed: Leppanen 2020 2-generation family, affected daughter/carrier mother F - Italy - - - - - LMPHM see paper; ... ANGPT2 ANGPT2 1 1 Audrey Debue
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