All individuals with variants in gene PMP2

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00473384 Fam207834Pat668 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history F no Iran - - - - - CMT Sporadic case , statrted 15y with climbing difficulty, pes cavus,distal lower and upper weakness and atrophy, paresthesia, chronic nonuniform demyelinating sensorimotor polyneuropathy reported in EDX. 1 1 Johan den Dunnen
00473858 Fam9802646Pat1356 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, family history M yes Iran - - - - - CMT onset 11y with difficulty walking; Difficulty climbing stairs and running; Distal muscle weakness, legs>arms; Pes cavus, bilateral; Ankle deformity, bilateral; Claw hallux, Rt; EMG-NCV: axonal and demyelinating sensory-motor polyneuropathy charcot-marie-tooth disease. 1 1 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.