All individuals with variants in gene TYMP

24 entries on 1 page. Showing entries 1 - 24.
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     
00037301 - - - - - Germany - - - - - ? suspected MNGIE 1 1 Andreas Laner
00037302 - - - - - Germany - - - - - ? suspected MNGIE 1 1 Andreas Laner
00037303 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00037304 - - - - - Germany - - - - - ? weight loss, demyelinating polyneuropathy, ophtalmoplegia, leukoencephalopathy 1 1 Andreas Laner
00037305 - - - - - Germany - - - - - ? suspected mitochondriopathy, status post purulent peritonitis, status post Ileus, hearing loss 1 1 Andreas Laner
00037306 - - - - - Germany - - - - - ? suspected MNGIE 1 1 Andreas Laner
00037307 - - - - - Germany - - - - - ? suspected MNGIE 1 1 Andreas Laner
00037308 - - - - - Germany - - - - - MEOAL;MMDS8 MNGIE 1 1 Andreas Laner
00050428 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected M - United Kingdom (Great Britain) - - - Decipher - ? generalized hypotonia, global developmental delay 1 1 Johan den Dunnen
00225598 - - - M - - - - - - - - HP:0001271 (Polyneuropathy) 1 1 Gunnar Schmidt
00250187 - - - F no United States - - - - - MTDPS1 Elevated thymidine, ptosis, PEO, peripheral neuropathy 2 1 Kimberly Kripps
00250188 - - - M no United States Navajo - - - - MTDPS1 Elevated thymidine, liver cirrhosis and failure, hearing loss 1 1 Kimberly Kripps
00250189 - - - F ? United States - - - - - MTDPS1 severe gastrointestinal dysmotility, fatigue, weakness, extremity paresthesias 1 1 Kimberly Kripps
00250190 - - - M ? United States - - - - - MTDPS1 demyelinating neuropathy, liver cirrhosis, gastric dysmotility 1 1 Kimberly Kripps
00293158 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00293159 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 5 Mohammed Faruq
00293160 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00296610 Pat43 PubMed: Taylor 2014 - F - United Kingdom (Great Britain) British <01m - - - ? deceased; muscle affected; central nervous system not affected; heart not affected; liver not affected; congenital lactic acidosis, mtDNA depletion 1 1 Johan den Dunnen
00320152 - - - F - - - - - - - ? Polycystic kidney dysplasia (HP:0000113); Microcephaly (HP:0000252); Global developmental delay (HP:0001263); Failure to thrive (HP:0001508); Broad toe (HP:0001837); Broad thumb (HP:0011304); Arachnoid cyst (HP:0100702) 1 1 IMGAG
00469483 - PubMed: Retterer 2016 analysis proband (1/3040); possible combination of variants not reported - - United States - - - - - ? - 1 1 Johan den Dunnen
00469484 - PubMed: Retterer 2016 analysis proband (1/3040); possible combination of variants not reported - - United States - - - - - ? - 1 1 Johan den Dunnen
00473135 Fam101296Pat269 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history M yes Iran - - - - - MYOP onset 21y with weight loss & digestive manifestations including malnutrition, malabsorption, vomiting, and chronic abdominal pain, suspicious of Crohn disease; Facial weakness; Ophthalmoplegia; Progressive proximal & distal muscle weakness & wasting; Pes cavus; Feet drop; Areflexia; Impaired walking, Imbalance; EMG-NCV: chronic demyelinating sensorimotor polyneuropathy. 1 1 Johan den Dunnen
00473426 Fam209859Pat731 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, family history F yes Iran - - - - - MYOP Bilateral ptosis, proximal and distal muscle weakness, paresthesia, inability toe-heel walking, mild facial weakness ,progressive external ophtalmoplegia, diabetes, chronic demyelinating sensorimotor polyneuropathy and evidence of irritable myopathy, mitochondrial myopathy reported in muscle biopsy. 1 1 Johan den Dunnen
00473445 Fam211181Pat760 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history M yes Iran - - - - - MYOP sporadic case, started since childhood with proximal and distal lower and upper muscle weakness, positive Gowers` sign, facial weakness, bilateral ptosis, chronic demyelinating sensorimotor poly neuropathy reported in EDX 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.