
 Phenotype ID
|

 Phenotype details
|

 Diagnosis/Initial
|

 Diagnosis/Definite
|

 Inheritance
|

 Age/Examination
|

 Age/Diagnosis
|

 Age/Onset
|

 Phenotype/Onset
|

 Protein
|

 Owner
|

 Individual ID
|
| 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 |