Disease #04024 (PPKN (keratoderma, palmoplantar, Nagashima type (PPKN)), OMIM:615598)

Official abbreviation PPKN
Name keratoderma, palmoplantar, Nagashima type (PPKN)
OMIM ID 615598
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene SERPINB7
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

1 entry on 1 page. Showing entry 1.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00460675 FamPatIII3 PubMed: Tan 2025 3-generation family, 5 affected (3F, 2M), seggregating BMD and FSHD M - China - - - - - MD, PPKN see paper; ..., see paper; ..., flushing, erythema, hyperkeratosis palmar surface hands/feet, see paper; ..., weakness eye/mouth orbicular muscles, shoulder muscles, proximal upper/lower limbs muscles; scoliosis; winged scapula; pseudohypertrophy gastrocnemius muscle; raised CK (5,006U/L) DMD DMD, DUX4, SERPINB7 4 5 Johan den Dunnen
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.