Disease #05101 (adermatoglyphia, congenital facial milia, acral blisters, digital contractures, nail abnormalities (Basan syndrome), OMIM:129200)

Official abbreviation -
Name adermatoglyphia, congenital facial milia, acral blisters, digital contractures, nail abnormalities (Basan syndrome)
OMIM ID 129200
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 0 genes -
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Disease features -
Remarks -
Date created 2015-11-10 10:55:30 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00054657 - - - F no China Chinese Han - - Pedigree No adermatoglyphia, congenital facial milia, acral blisters, digital contractures, nail abnormalities (Basan syndrome) Basan Syndrome SMARCAD1 GRID2 1 1 Ming Li
00057917 - - - F no China - 03y - - - adermatoglyphia, congenital facial milia, acral blisters, digital contractures, nail abnormalities (Basan syndrome) Basan syndrome SMARCAD1 - - 1 Ming Li
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