Disease #00606 (mitochondrial respiratory chain complex II deficiency, OMIM:252011)

Official abbreviation -
Name mitochondrial respiratory chain complex II deficiency
OMIM ID 252011
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 3 genes SDHA, SDHAF1, SDHD
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

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00443794 - - - - - - - - - - - mitochondrial respiratory chain complex II deficiency psychomotor retardation cognitive impairment cerebral and cerebellar atrophy bulbar signs ophthalmoparesis nystagmus sensorineural hearing impairment PTPMT1 PTPMT1 1 1 Ece Sonmezler
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