Phenotypes for disease #02477 (MLC (leukoencephalopathy, megalencephalic, with subcortical cysts (MLC)))

607 entries on 7 pages. Showing entries 1 - 100.
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0000331161 normal initial cognitive development; normal initial motor development; 9m-increased OFC; never walked; 4y-start motor decline; 6y-full wheelchair dependency; 4y-start cognitive decline; rage; no history psychiatric diagnoses; 4y-refractory generalized seizures; no status epilepticus; OFC >+2SD; clumsiness; spasticity of arms; spasticity of legs; no gait/truncal ataxia; no appendicular ataxia; no dystonia; no rigidity; dysarthria; no dysphagia; severe cognitive deficit brain oedema MLC3 Isolated (sporadic) 19y - - - - Rogier Min 00441736
0000331162 mildly delayed initial cognitive development; mildly delayed initial motor development; 7m-increased OFC; 3y-walk; 4y-start motor decline; 5y-loss unsupported walking; 6y-full wheelchair dependency; 15y-start cognitive decline; no behavioural problems; no history psychiatric diagnoses; 14y-occasional generalized seizures; OFC 62 cm (>+2SD); clumsiness; spasticity of arms; spasticity of legs; gait/truncal ataxia; appendicular ataxia; dystonia; dysarthria; dysphagia; mild cognitive deficit; no autistic features brain oedema MLC3 Isolated (sporadic) 27y - - - - Rogier Min 00441737
0000331163 normal initial cognitive development; normal initial motor development; 6m-increased OFC; 13m-walk; 8y-start motor decline; 8y-loss unsupported walking; 12y-full wheelchair dependency; 14y-start cognitive decline; no behavioural problems; 14y-depression; two single seizures after fall (adulthood); no status epilepticus; OFC 61.5 cm (>+2SD); clumsiness; spasticity of arms; spasticity of legs; gait/truncal ataxia; appendicular ataxia; no dystonia; rigidity; dysarthria; no dysphagia; mild cognitive deficit; no autistic features brain oedema MLC3 Isolated (sporadic) 24y - - - - Rogier Min 00441738
0000331164 highly delayed initial cognitive development; highly delayed initial motor development; 6m-increased OFC; 4-5y-walk; no cognitive decline; in childhood agitation, impulsivity, hyperactivity and sleep disorder, later improvement; no history psychiatric diagnoses; 1y-severe epilepsy; frequent status epilepticus; OFC 57.5cm (normal); clumsiness; no spasticity of arms; no spasticity of legs; gait/truncal ataxia; appendicular ataxia; dystonia; mild rigidity; dysarthria; no dysphagia; severe cognitive deficit; no autistic features brain oedema MLC4 Familial, autosomal recessive 16y - - - - Rogier Min 00441739
0000331165 mildly delayed initial cognitive development; highly delayed initial motor development; 6m-increased OFC; 2y-walk; no cognitive decline; impulsivity, hyperactivity in early childhood, later normalization; no history psychiatric diagnoses; 1y-occasional generalized seizures; no status epilepticus; OFC 58 cm (>+2SD); clumsiness; no spasticity of arms; no spasticity of legs; no gait/truncal ataxia; no appendicular ataxia; no dystonia; no rigidity; no dysarthria; mild cognitive deficit; no autistic features brain oedema MLC4 Familial, autosomal recessive 13y - - - - Rogier Min 00441740
0000331336 macrocephaly; normal early motor development; 18m-walk; normal language development; 2y-detoriation; ataxia, spasticity,; late cognitive; decline; 7y-wheelchair-bound; 11y-seizures; intellectual disability (IQ50); OFC >98perc.; dysarthria; dysphagia; spasticity arms; cerebellar ataxia arms; spasticity legs classical megalencephalic leukoencephalopathy with subcortical cysts MLC2A Familial, autosomal recessive 38y - 1y - - Rogier Min 00441953
0000331337 macrocephaly; mildly delayed early motor development; 24m-walk; normal language development; 5y6m-detoriation; ataxia, spasticity,; dystonia, late mild; cognitive decline; 14y-wheelchair-bound; 32y-seizures; intellectual disability (IQ75); OFC >98perc.; dysarthria; dysphagia; spasticity arms; cerebellar ataxia arms; spasticity legs; cerebellar ataxia legs classical megalencephalic leukoencephalopathy with subcortical cysts MLC2A Familial, autosomal recessive 37y - <1y - - Rogier Min 00441954
0000331338 ataxia; normal early motor development; 18m-walk; normal language development; 3y-detoriation; ataxia; still ambulant; no seizures; no intellectual disability; OFC >98perc.; no dysarthria; no dysphagia; no spasticity arms; no cerebellar ataxia arms; no spasticity legs; cerebellar ataxia legs classical megalencephalic leukoencephalopathy with subcortical cysts MLC2A Familial, autosomal recessive 18y - <3y - - Rogier Min 00441955
0000331339 macrocephaly; delayed early motor development; 24m-walk; normal language development; 7y-detoriation; loss of speech; tube feeding; 7y-wheelchair-bound; 2y-seizures; intellectual disability (IQ50); OFC >98perc.; dysarthria; dysphagia; spasticity arms; cerebellar ataxia arms; spasticity legs classical megalencephalic leukoencephalopathy with subcortical cysts MLC2A Familial, autosomal recessive 13y - 1y - - Rogier Min 00441956
0000331340 macrocephaly; normal early motor development; 14m-walk; normal language development; 4y-detoriation; ataxia, dysarthria, ataxia, dysarthria; 7y-wheelchair-bound; 3y-seizures; intellectual disability (IQ75); OFC >98perc.; dysarthria; dysphagia; spasticity arms; cerebellar ataxia arms; spasticity legs; cerebellar ataxia legs classical megalencephalic leukoencephalopathy with subcortical cysts MLC2A Familial, autosomal recessive 10y - 3m - - Rogier Min 00441957
0000331341 macrocephaly; normal early motor development; 15m-walk; normal language development; 4y-detoriation; spasticity; still ambulant; 4y-seizures; intellectual disability (IQ70); OFC >98perc.; no dysarthria; no dysphagia; no spasticity arms; no cerebellar ataxia arms; spasticity legs; no cerebellar ataxia legs classical megalencephalic leukoencephalopathy with subcortical cysts MLC2A Familial, autosomal recessive 7y6m - 1d - - Rogier Min 00441958
0000331342 macrocephaly; normal early motor development; 17m-walk; normal language development; 17m-detoriation; spasticity; still ambulant; no seizures; intellectual disability (IQ70); OFC >98perc.; no dysarthria; no dysphagia; no spasticity arms; no cerebellar ataxia arms; spasticity legs; no cerebellar ataxia legs classical megalencephalic leukoencephalopathy with subcortical cysts MLC2A Familial, autosomal recessive 11y - 1d - - Rogier Min 00441959
0000331343 febrile seizure; normal early motor development; 14m-walk; normal language development; 1y-detoriation; ataxia,; seizures; still ambulant; 1y-seizures; intellectual disability (IQ55); OFC >98perc.; dysarthria; no dysphagia; no spasticity arms; cerebellar ataxia arms; no spasticity legs; cerebellar ataxia legs classical megalencephalic leukoencephalopathy with subcortical cysts MLC2A Familial, autosomal recessive 8y - 1y - - Rogier Min 00441960
0000331344 macrocephaly; mildly delayed early motor development; 26m-walk; delayed language development; 3y-detoriation; seizures,; cognitive; decline; still ambulant; 3y-seizures; OFC >98perc.; dysarthria; no dysphagia; no spasticity arms; cerebellar ataxia arms; spasticity legs; cerebellar ataxia legs classical megalencephalic leukoencephalopathy with subcortical cysts MLC2A Familial, autosomal recessive 6y - <1y - - Rogier Min 00441961
0000331345 macrocephaly; mildly delayed early motor development; 16m-walk; mildly delayed language development; no detoriation; still ambulant; 2y-seizures; intellectual disability (IQ60); OFC >98perc.; dysarthria; no dysphagia; no spasticity arms; cerebellar ataxia arms; no spasticity legs; cerebellar ataxia legs classical megalencephalic leukoencephalopathy with subcortical cysts MLC2A Familial, autosomal recessive 5y - 1d - - Rogier Min 00441962
0000331346 macrocephaly; delayed early motor development; 16m-walk; normal language development; no epilepsy; no autism; no deterioration; no intellectual disability; OFC >98perc.; cranial nerves normal; no hypotonia arms; no motor signsarms; no hypotonia legs; no motor signs legs improving megalencephalic leukoencephalopathy with subcortical cysts phenotype MLC2B Unknown 13y - 5m - - Rogier Min 00441963
0000331347 macrocephaly; normal early motor development; normal language development; no epilepsy; no autism; no deterioration; no intellectual disability; OFC >98perc.; cranial nerves normal; no hypotonia arms; no motor signsarms; no hypotonia legs; no motor signs legs improving megalencephalic leukoencephalopathy with subcortical cysts phenotype MLC2B Unknown 12y - 8m - - Rogier Min 00441964
0000331348 transient macrocephaly; delayed early motor development; 22m-walk; normal language development; no epilepsy; no autism; no deterioration; no intellectual disability; cranial nerves normal; no hypotonia arms; clumsy with arms; no hypotonia legs; clumsy with legs improving megalencephalic leukoencephalopathy with subcortical cysts phenotype MLC2B Unknown 10y - 6m - - Rogier Min 00441965
0000331349 macrocephaly; delayed early motor development; 18m-walk; no speech; no epilepsy; autism; no deterioration; intellectual disability (IQ50); OFC now 60->98perc.; cranial nerves normal; no hypotonia arms; no hypotonia legs improving megalencephalic leukoencephalopathy with subcortical cysts phenotype MLC2B Unknown 12y - 4m - - Rogier Min 00441966
0000331350 3y6m-deceased (seizures); seizures, macrocephaly; delayed early motor development; 20m-walk; delayed language development; epilepsy; no autism; no deterioration; intellectual disability (IQ50); OFC >98perc.; cranial nerves normal; hypotonia arms; clumsy with arms; hypotonia legs; clumsy with legs improving megalencephalic leukoencephalopathy with subcortical cysts phenotype MLC2B Unknown 3y - 4m - - Rogier Min 00441967
0000331351 macrocephaly; delayed early motor development; 17m-walk; delayed language development; no epilepsy; no autism; no deterioration; intellectual disability (IQ75); OFC 90perc.; cranial nerves normal; no hypotonia arms; clumsy with arms; no hypotonia legs; clumsy with legs improving megalencephalic leukoencephalopathy with subcortical cysts phenotype MLC2B Unknown 6y - 6m - - Rogier Min 00441968
0000331352 macrocephaly, delay; delayed early motor development; 14m-walk; delayed language development; no epilepsy; no autism; no deterioration; no intellectual disability; OFC >98perc.; cranial nerves normal; mild hypotonia arms; no motor signsarms; mild hypotonia legs; no motor signs legs improving megalencephalic leukoencephalopathy with subcortical cysts phenotype MLC2B Unknown 8y6m - 7m - - Rogier Min 00441969
0000331353 macrocephaly, delay; delayed early motor development; 17m-walk; delayed language development; no epilepsy; no autism; no deterioration; no intellectual disability; OFC >98perc.; cranial nerves normal; mild hypotonia arms; no motor signsarms; mild hypotonia legs; no motor signs legs improving megalencephalic leukoencephalopathy with subcortical cysts phenotype MLC2B Unknown 5y6m - 4m - - Rogier Min 00441970
0000331354 macrocephaly; delayed early motor development; 13m-walk; normal language development; no epilepsy; no autism; no deterioration; no intellectual disability; OFC >98perc.; cranial nerves normal; no hypotonia arms; clumsy with arms; mild hypotonia legs; no motor signs legs improving megalencephalic leukoencephalopathy with subcortical cysts phenotype MLC2B Unknown 9y6m - 11m - - Rogier Min 00441971
0000331355 macrocephaly; normal early motor development; 14m-walk; normal language development; no epilepsy; no autism; no deterioration; no intellectual disability; OFC >98perc.; cranial nerves normal; no hypotonia arms; clumsy with arms; no hypotonia legs; clumsy with legs improving megalencephalic leukoencephalopathy with subcortical cysts phenotype MLC2B Unknown 6½y - 9m - - Rogier Min 00441972
0000331356 macrocephaly; normal early motor development; 16m-walk; delayed language development; no epilepsy; no autism; no deterioration; intellectual disability (IQ50); OFC >98perc.; cranial nerves normal; no hypotonia arms; no motor signsarms; no hypotonia legs; no motor signs legs improving megalencephalic leukoencephalopathy with subcortical cysts phenotype MLC2B Unknown 6y - 6m - - Rogier Min 00441973
0000331357 perinatal problems, small for gestational age, microcephaly, hypotonia; delayed early motor development; 32m-walk; delayed language development; no epilepsy; no autism; no deterioration; intellectual disability (IQ50); OFC >98perc.; cranial nerves normal; mild hypotonia arms; clumsy with arms; mild hypotonia legs; no motor signs legs improving megalencephalic leukoencephalopathy with subcortical cysts phenotype MLC2B Unknown 5y6m - 1d - - Rogier Min 00441974
0000331358 macrocephaly; normal early motor development; 14m-walk; delayed language development; no epilepsy; autism; no deterioration; intellectual disability (IQ50); OFC >98perc.; mild hypotonia arms; no motor signsarms; mild hypotonia legs; no motor signs legs improving megalencephalic leukoencephalopathy with subcortical cysts phenotype MLC2B Unknown 2y9m - 4m - - Rogier Min 00441975
0000331359 macrocephaly; normal early motor development; 16m-walk; normal language development; no epilepsy; no autism; no deterioration; no intellectual disability; OFC >98perc.; dysarthria NL; no hypotonia arms; no motor signsarms; no hypotonia legs; no motor signs legs improving megalencephalic leukoencephalopathy with subcortical cysts phenotype MLC2B Unknown 5y - 4m - - Rogier Min 00441976
0000331360 transient macrocephaly; delayed early motor development; 18m-walk; normal language development; no epilepsy; no autism; no deterioration; no intellectual disability; OFC 75perc.; cranial nerves normal; no hypotonia arms; no motor signsarms; no hypotonia legs; no motor signs legs improving megalencephalic leukoencephalopathy with subcortical cysts phenotype MLC2B Unknown 3y - 8m - - Rogier Min 00441977
0000331361 macrocephaly; normal early motor development; 14m-walk; delayed language development; no epilepsy; autism; no deterioration; intellectual disability (IQ70); OFC >98perc.; cranial nerves normal; mild hypotonia arms; no motor signsarms; mild hypotonia legs; no motor signs legs improving megalencephalic leukoencephalopathy with subcortical cysts phenotype MLC2B Unknown 2y - 3m - - Rogier Min 00441978
0000331362 macrocephaly; delayed early motor development; 22m-walk; delayed language development; no epilepsy; no autism; no deterioration; no intellectual disability; OFC >98perc.; cranial nerves normal; no hypotonia arms; no motor signsarms; no hypotonia legs; no motor signs legs improving megalencephalic leukoencephalopathy with subcortical cysts phenotype MLC2B Unknown 2y9m - 7m - - Rogier Min 00441979
0000331363 macrocephaly; normal early motor development; 14m-walk; normal language development; no epilepsy; no autism; no deterioration; no intellectual disability; OFC >98perc.; cranial nerves normal; no hypotonia arms; no motor signsarms; no hypotonia legs; no motor signs legs improving megalencephalic leukoencephalopathy with subcortical cysts phenotype MLC2B Unknown 1y6m - 5m - - Rogier Min 00441980
0000331364 - megalencephalic leukoencephalopathy with subcortical cysts MLC2A Familial, autosomal recessive - - - - - Rogier Min 00441981
0000331365 - megalencephalic leukoencephalopathy with subcortical cysts MLC2B Familial, autosomal dominant - - - - - Rogier Min 00441982
0000331366 - megalencephalic leukoencephalopathy with subcortical cysts MLC2B Familial, autosomal dominant - - - - - Rogier Min 00441983
0000331367 - megalencephalic leukoencephalopathy with subcortical cysts MLC2B Familial, autosomal dominant - - - - - Rogier Min 00441984
0000331368 - megalencephalic leukoencephalopathy with subcortical cysts MLC2B Familial, autosomal dominant - - - - - Rogier Min 00441985
0000331369 - megalencephalic leukoencephalopathy with subcortical cysts MLC2B Familial, autosomal dominant - - - - - Rogier Min 00441986
0000331370 - megalencephalic leukoencephalopathy with subcortical cysts MLC2A Familial, autosomal recessive - - - - - Rogier Min 00441987
0000331371 - megalencephalic leukoencephalopathy with subcortical cysts MLC2A Familial, autosomal recessive - - - - - Rogier Min 00441988
0000331372 - megalencephalic leukoencephalopathy with subcortical cysts MLC2A Familial, autosomal recessive - - - - - Rogier Min 00441989
0000331373 - megalencephalic leukoencephalopathy with subcortical cysts MLC2B Familial, autosomal dominant - - - - - Rogier Min 00441990
0000331374 - megalencephalic leukoencephalopathy with subcortical cysts MLC2B Familial, autosomal dominant - - - - - Rogier Min 00441991
0000331375 - megalencephalic leukoencephalopathy with subcortical cysts MLC2B Familial, autosomal dominant - - - - - Rogier Min 00441992
0000331376 - megalencephalic leukoencephalopathy with subcortical cysts MLC2A Familial, autosomal recessive - - - - - Rogier Min 00441993
0000331377 - megalencephalic leukoencephalopathy with subcortical cysts MLC2B Familial, autosomal dominant - - - - - Rogier Min 00441994
0000331378 - megalencephalic leukoencephalopathy with subcortical cysts MLC2A Familial, autosomal recessive - - - - - Rogier Min 00441995
0000331379 - megalencephalic leukoencephalopathy with subcortical cysts MLC2B Familial, autosomal dominant - - - - - Rogier Min 00441996
0000331380 - megalencephalic leukoencephalopathy with subcortical cysts MLC2B Familial, autosomal dominant - - - - - Rogier Min 00441997
0000331381 - megalencephalic leukoencephalopathy with subcortical cysts MLC2A Familial, autosomal recessive - - - - - Rogier Min 00441998
0000331382 - megalencephalic leukoencephalopathy with subcortical cysts MLC2B Familial, autosomal dominant - - - - - Rogier Min 00441999
0000331383 - megalencephalic leukoencephalopathy with subcortical cysts MLC2B Familial, autosomal dominant - - - - - Rogier Min 00442000
0000331384 - megalencephalic leukoencephalopathy with subcortical cysts MLC2B Familial, autosomal dominant - - - - - Rogier Min 00442001
0000331385 - megalencephalic leukoencephalopathy with subcortical cysts MLC2B Familial, autosomal dominant - - - - - Rogier Min 00442002
0000331386 - megalencephalic leukoencephalopathy with subcortical cysts MLC2B Familial, autosomal dominant - - - - - Rogier Min 00442003
0000331387 - megalencephalic leukoencephalopathy with subcortical cysts MLC2B Familial, autosomal dominant - - - - - Rogier Min 00442004
0000331388 - megalencephalic leukoencephalopathy with subcortical cysts MLC2B Familial, autosomal dominant - - - - - Rogier Min 00442005
0000331389 - megalencephalic leukoencephalopathy with subcortical cysts MLC2B Familial, autosomal dominant - - - - - Rogier Min 00442006
0000331390 - megalencephalic leukoencephalopathy with subcortical cysts MLC2A Familial, autosomal recessive - - - - - Rogier Min 00442007
0000331391 - megalencephalic leukoencephalopathy with subcortical cysts MLC2B Familial, autosomal dominant - - - - - Rogier Min 00442008
0000331392 - megalencephalic leukoencephalopathy with subcortical cysts MLC2A Familial, autosomal recessive - - - - - Rogier Min 00442009
0000331393 - megalencephalic leukoencephalopathy with subcortical cysts MLC2B Familial, autosomal dominant - - - - - Rogier Min 00442010
0000331394 - megalencephalic leukoencephalopathy with subcortical cysts MLC2B Familial, autosomal dominant - - - - - Rogier Min 00442011
0000331395 - megalencephalic leukoencephalopathy with subcortical cysts MLC2A Familial, autosomal recessive - - - - - Rogier Min 00442012
0000331396 - megalencephalic leukoencephalopathy with subcortical cysts MLC2B Familial, autosomal dominant - - - - - Rogier Min 00442013
0000331397 - megalencephalic leukoencephalopathy with subcortical cysts MLC2A Familial, autosomal recessive - - - - - Rogier Min 00442014
0000331398 - megalencephalic leukoencephalopathy with subcortical cysts MLC2B Familial, autosomal dominant - - - - - Rogier Min 00442015
0000331400 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442017
0000331401 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442018
0000331402 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442019
0000331403 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442020
0000331404 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442021
0000331405 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442022
0000331406 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442023
0000331407 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442024
0000331408 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442025
0000331409 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442026
0000331410 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442027
0000331411 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442028
0000331412 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442029
0000331413 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442030
0000331414 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442031
0000331415 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442032
0000331416 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442033
0000331417 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442034
0000331418 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442035
0000331419 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442036
0000331420 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442037
0000331421 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442038
0000331422 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442039
0000331423 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442040
0000331424 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442041
0000331425 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442042
0000331426 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442043
0000331427 see paper; ... megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442044
0000331429 - megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442063
0000331430 - megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442064
0000331431 s megalencephalic leukoencephalopathy with subcortical cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442065
0000331432 see paper; ... Agarwal megalencephalic leukodystrophy with cysts MLC1 Familial, autosomal recessive - - - - - Johan den Dunnen 00442072
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