Disease #02794 (HLD2;PMLD1 (leukodystrophy, hypomyelinating, type 2 (HLD-2, Pelizaeus-Merzbacher like disease 1 (PMLD-1))), OMIM:608804)

Official abbreviation HLD2;PMLD1
Name leukodystrophy, hypomyelinating, type 2 (HLD-2, Pelizaeus-Merzbacher like disease 1 (PMLD-1))
OMIM ID 608804
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 7
Phenotype entries for this disease 7
Associated with 1 gene GJC2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

7 entries on 1 page. Showing entries 1 - 7.
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00055368 - - - - - - - - - - - HLD2;PMLD1 Pelizaeus-Merzbacher like disease GJC2 GJC2 2 1 Michel van Geel
00055369 - - - - - - - - - - - HLD2;PMLD1 Pelizaeus-Merzbacher like disease GJC2 GJC2 2 1 Michel van Geel
00055370 - - - - - - - - - - - HLD2;PMLD1 Pelizaeus-Merzbacher like disease GJC2 GJC2 2 1 Michel van Geel
00055371 - - 2 affecteds sibs - yes Pakistan - - - - - HLD2;PMLD1 Pelizaeus-Merzbacher like disease GJC2 GJC2 2 2 Michel van Geel
00055372 - - - - yes Pakistan - - - - - HLD2;PMLD1 Pelizaeus-Merzbacher like disease GJC2 GJC2 2 2 Michel van Geel
00055373 - - - - - Algeria - - - - - HLD2;PMLD1 Pelizaeus-Merzbacher like disease GJC2 GJC2 2 1 Michel van Geel
00055374 - - - - - Algeria - - - - - HLD2;PMLD1 Pelizaeus-Merzbacher like disease GJC2 GJC2 2 1 Michel van Geel
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