Disease #02326 (NEPPK (keratoderma, palmoplantar, nonepidermolytic (NEPPK)), OMIM:600962)

Official abbreviation NEPPK
Name keratoderma, palmoplantar, nonepidermolytic (NEPPK)
OMIM ID 600962
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 6
Phenotype entries for this disease 6
Associated with 1 gene KRT1
Associated tissues -
Disease features -
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Individuals

6 entries on 1 page. Showing entries 1 - 6.
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00055405 - - - - - - - - 0 - - NEPPK keratoderma, non-epidermolytic palmoplantar KRT1 KRT1 1 1 Michel van Geel
00055455 - - Family 2 - - - - - 0 - - NEPPK keratoderma, non-epidermolytic palmoplantar KRT1 KRT1 1 1 Michel van Geel
00055456 - - Family 1 - - - - - 0 - - NEPPK keratoderma, non-epidermolytic palmoplantar KRT1 KRT1 1 1 Michel van Geel
00055457 - - Family 3 - - - - - 0 - - NEPPK keratoderma, non-epidermolytic palmoplantar KRT1 KRT1 1 1 Michel van Geel
00055458 - - - - - China - - 0 - - NEPPK keratoderma, non-epidermolytic palmoplantar KRT1 KRT1 1 1 Michel van Geel
00208752 30452289-Fam PubMed: Tang 2018 4-generation family, 13 affected (9F, 4M) F;M no China - - 0 - - NEPPK see paper; ... KRT1 KRT1 1 13 Johan den Dunnen
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