Disease #01394 (IHCM (ichthyosis hystrix, Curth-Macklin type (IHCM)), OMIM:146590)

Official abbreviation IHCM
Name ichthyosis hystrix, Curth-Macklin type (IHCM)
OMIM ID 146590
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 1 gene KRT1
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

5 entries on 1 page. Showing entries 1 - 5.
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00055415 - - - - - United States - 1y - - - IHCM - KRT1 KRT1 1 1 Michel van Geel
00055439 - - - M - United States African-American - - - - IHCM - KRT1 KRT1 1 1 Michel van Geel
00055441 - - - - - - - - - - - IHCM - KRT1 KRT1 1 1 Michel van Geel
00055857 - - - M - Japan - - - - - IHCM collodion-like baby KRT1 KRT1 1 1 Johan den Dunnen
00055861 - - family, 2 affected F - Colombia - - - - - IHCM - KRT1 KRT1 1 2 Johan den Dunnen
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