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*620769 - HYDROXYACYL-THIOESTER DEHYDRATASE, TYPE 2; HTD2
Gene summaries Genetic tests Medical literature
*620765 - MITOCHONDRIAL FISSION REGULATOR 1-LIKE PROTEIN; MTFR1L
*620737 - COENZYME Q10B; COQ10B
*620736 - COENZYME Q10A; COQ10A
*620735 - SERINE DEHYDRATASE-LIKE PROTEIN; SDSL
#620732 - NEURODEVELOPMENTAL DISORDER WITH HYPERKINETIC MOVEMENTS, SEIZURES, AND STRUCTURAL BRAIN ABNORMALITIES; NEDMSB
#620729 - HYPERFERRITINEMIA; HRFT
#620728 - ULLRICH CONGENITAL MUSCULAR DYSTROPHY 1C; UCMD1C
#620727 - ULLRICH CONGENITAL MUSCULAR DYSTROPHY 1B; UCMD1B
ULLRICH CONGENITAL MUSCULAR DYSTROPHY 1A/1B, DIGENIC, INCLUDED; UCMD1A/1B, DIGENIC, INCLUDED
#620726 - BETHLEM MYOPATHY 1C; BTHLM1C
#620725 - BETHLEM MYOPATHY 1B; BTHLM1B
*620724 - ENOYL COENZYME A HYDRATASE DOMAIN-CONTAINING PROTEIN 2; ECHDC2
#620722 - DEAFNESS, AUTOSOMAL DOMINANT 90; DFNA90
#620718 - OROFACIODIGITAL SYNDROME XX; OFD20
#620711 - LEUKOENCEPHALOPATHY, PORPHYRIA-RELATED; LENCEP
#620705 - SPERMATOGENIC FAILURE 89; SPGF89
#620704 - ENCEPHALOPATHY, PORPHYRIA-RELATED; ENCEP
#620700 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 81; MRT81
#620699 - MAPLE SYRUP URINE DISEASE, TYPE II; MSUD2
#620698 - MAPLE SYRUP URINE DISEASE, TYPE IB; MSUD1B
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