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Neurometabolic Diseases Laboratory (Bellvitge Biomedical Research Institute (IDIBELL))

General information

Neurometabolic Diseases Laboratory
Bellvitge Biomedical Research Institute (IDIBELL)
Hospitalet del Llobregat
Spain

Organization ID: 509068

Personnel

Assertion criteria

Level: Assertion criteria provided

Summary of submissions to ClinVar

Total submissions: 106

Gene

GeneSubmissionsLast Updated
ACER31Apr 28, 2023
AFG3L21Apr 28, 2023
ALS21Apr 28, 2023
AMPD21Apr 28, 2023
AP4B12Apr 28, 2023
AP4B1-AS11Apr 28, 2023
ATL13Apr 28, 2023
BCKDK1Apr 28, 2023
BSCL21Apr 28, 2023
CACNA1A2Apr 28, 2023
CAPN11Apr 28, 2023
CAPN101Apr 28, 2023
CC2D2A2Apr 28, 2023
COL6A31Apr 28, 2023
CTNNB11Apr 28, 2023
CYP2U11Apr 28, 2023
DDHD21Apr 28, 2023
DLG41Apr 28, 2023
DSTYK1Apr 28, 2023
ERBB41Apr 28, 2023
FA2H1Apr 28, 2023
FARS22Apr 28, 2023
GFAP1Apr 28, 2023
HNRNPUL2-BSCL21Apr 28, 2023
IFIH12Apr 28, 2023
IQSEC21Apr 28, 2023
IRF2BPL1Apr 28, 2023
KCNA11Apr 28, 2023
KIDINS2201Apr 28, 2023
KIF1A3Apr 28, 2023
KIF5A1Apr 28, 2023
KMT2B1Apr 28, 2023
L2HGDH1Apr 28, 2023
LAMA12Apr 28, 2023
LOC1125434341Apr 28, 2023
LOC1268609711Apr 28, 2023
LOC1299923301Apr 28, 2023
LONP12Apr 28, 2023
MMUT1Apr 28, 2023
MORC21Apr 28, 2023
NDUFS61Apr 28, 2023
PAX61Apr 28, 2023
PCYT21Apr 28, 2023
PDK31Apr 28, 2023
PI4KA4Apr 28, 2023
PMM22Apr 28, 2023
PNKP2Apr 28, 2023
PNPLA62Apr 28, 2023
POLG2Apr 28, 2023
POLGARF2Apr 28, 2023
POLR1C1Apr 28, 2023
POLR3A7Apr 28, 2023
POLR3B1Apr 28, 2023
REEP12Apr 28, 2023
RINT13Apr 28, 2023
RNASEH2B1Apr 28, 2023
SARS11Apr 28, 2023
SEPSECS1Apr 28, 2023
SHMT21Apr 28, 2023
SLC25A461Apr 28, 2023
SLC35B21Apr 28, 2023
SPAST4Apr 28, 2023
SPG118Apr 28, 2023
SPG75Apr 28, 2023
SPTAN11Apr 28, 2023
SPTBN21Apr 28, 2023
SVBP1Apr 28, 2023
TAF11Apr 28, 2023
TMEM2401Apr 28, 2023
TRMT52Apr 28, 2023
UBAP11Apr 28, 2023

Condition

NameSubmissionsLast Updated
Aicardi-Goutieres syndrome 21Apr 28, 2023
Aicardi-Goutieres syndrome 72Apr 28, 2023
Alkaline ceramidase 3 deficiency1Apr 28, 2023
Amyotrophic lateral sclerosis type 191Apr 28, 2023
Ataxia - oculomotor apraxia type 42Apr 28, 2023
Autosomal recessive spastic paraplegia type 761Apr 28, 2023
Branched-chain keto acid dehydrogenase kinase deficiency1Apr 28, 2023
CAPN10-related disorder1Apr 28, 2023
COL6A3-related disorder1Apr 28, 2023
Charcot-Marie-Tooth disease X-linked dominant 61Apr 28, 2023
Combined oxidative phosphorylation defect type 142Apr 28, 2023
Combined oxidative phosphorylation defect type 262Apr 28, 2023
Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy1Apr 28, 2023
Dystonia 28, childhood-onset1Apr 28, 2023
Episodic ataxia type 11Apr 28, 2023
GFAP-related disorder1Apr 28, 2023
Hereditary spastic paraplegia 101Apr 28, 2023
Hereditary spastic paraplegia 118Apr 28, 2023
Hereditary spastic paraplegia 171Apr 28, 2023
Hereditary spastic paraplegia 231Apr 28, 2023
Hereditary spastic paraplegia 303Apr 28, 2023
Hereditary spastic paraplegia 312Apr 28, 2023
Hereditary spastic paraplegia 351Apr 28, 2023
Hereditary spastic paraplegia 392Apr 28, 2023
Hereditary spastic paraplegia 3A3Apr 28, 2023
Hereditary spastic paraplegia 44Apr 28, 2023
Hereditary spastic paraplegia 472Apr 28, 2023
Hereditary spastic paraplegia 541Apr 28, 2023
Hereditary spastic paraplegia 561Apr 28, 2023
Hereditary spastic paraplegia 631Apr 28, 2023
Hereditary spastic paraplegia 75Apr 28, 2023
Infantile-onset ascending hereditary spastic paralysis1Apr 28, 2023
Intellectual developmental disorder 621Apr 28, 2023
Intellectual disability, X-linked 11Apr 28, 2023
Intellectual disability, X-linked, syndromic 331Apr 28, 2023
Joubert syndrome 92Apr 28, 2023
KCNA1-related disorder1Apr 28, 2023
L-2-hydroxyglutaric aciduria1Apr 28, 2023
LAMA1-related disorder2Apr 28, 2023
LONP1-related disorder2Apr 28, 2023
Leukodystrophy, hypomyelinating, 26, with chondrodysplasia1Apr 28, 2023
Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency1Apr 28, 2023
Mitochondrial complex 1 deficiency, nuclear type 91Apr 28, 2023
Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities1Apr 28, 2023
Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures1Apr 28, 2023
Neuropathy, hereditary motor and sensory, type 6B1Apr 28, 2023
PAX6-related disorder1Apr 28, 2023
PMM2-congenital disorder of glycosylation2Apr 28, 2023
POLG-related disorder2Apr 28, 2023
POLR3A-related disorder7Apr 28, 2023
POLR3B-related disorder1Apr 28, 2023
Pontocerebellar hypoplasia type 2D1Apr 28, 2023
RINT1-related disorder3Apr 28, 2023
SARS1-related disorder1Apr 28, 2023
SPTAN1-related disorder1Apr 28, 2023
SVBP-related disorder1Apr 28, 2023
Severe intellectual disability-progressive spastic diplegia syndrome1Apr 28, 2023
Spastic ataxia 51Apr 28, 2023
Spastic paraplegia 80, autosomal dominant1Apr 28, 2023
Spastic paraplegia 82, autosomal recessive1Apr 28, 2023
Spastic paraplegia 84, autosomal recessive4Apr 28, 2023
Spinocerebellar ataxia type 211Apr 28, 2023
Spinocerebellar ataxia type 51Apr 28, 2023
Spinocerebellar ataxia type 62Apr 28, 2023