Disease #04157 (dystrophy, bullous, hereditary, macular type (EBM), OMIM:302000)

Official abbreviation -
Name dystrophy, bullous, hereditary, macular type (EBM)
OMIM ID 302000
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -
Date created 2014-12-12 13:47:23 +01:00 (CET)
Date last edited N/A


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00025475 - - - M - Netherlands white - - - - dystrophy, bullous, hereditary, macular type (EBM) hereditary bullous dystrophy of the macular type HAUS7 HAUS7 1 3 Najim Ameziane
00025476 - - - M - Italy white - - - - dystrophy, bullous, hereditary, macular type (EBM) hereditary bullous dystrophy of the macular type HAUS7 HAUS7 1 1 Najim Ameziane
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