All individuals with variants in gene HACE1

3 entries on 1 page. Showing entries 1 - 3.
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     
00415277 32 PubMed: Alfares 2018 - F - - - - - - - retinal disease OMIM: 616756; intellectual disability, spasticity, and neurogenic bladder 1 1 LOVD
00444511 Pat13 PubMed: Riquin 2023 patient M - France - - - - - NDD Myoclonic epilepsy, encephalopathy, axial hypotonia, languange acquisition then regression, cortical atrophy on cerebral MRI, myelinisation delay, thin corpus callosum 2 1 Johan den Dunnen
00473803 Fam9703022Pat1271 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history F yes Iran - - - - - ? Hypotonia; Developmental retardation; Speech difficulty; CDH bilateral; Mild deep set eyes; Muscle biopsy: slight myopathic atrophy of mainly type 1 fibers with no specific structural abnormality; Brain MRI: bilateral cortical atrophy and agenesis of corpus callosum; EMG-NCV: myopathic process; Rectal biopsy: R/O Hirschsprung’s disease; Urine organic acid: slightly elevated lactic acid. 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.