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Disease association ontology term - MONDO:0005560 - brain disorder

Term summary

ID
MONDO:0005560
Name
brain disorder
Ontology or CV name
Disease association
Definition
A disease affecting the brain or part of the brain.

Parents

Annotation

Disease association

MONDO:0014744 - acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome

References:

Genes:

MONDO:0014557 - ataxia - oculomotor apraxia type 4

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MONDO:0008840 - ataxia telangiectasia

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MONDO:0011397 - autosomal dominant cerebellar ataxia, deafness and narcolepsy

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MONDO:0012784 - autosomal recessive ataxia due to ubiquinone deficiency

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MONDO:0015244 - autosomal recessive cerebellar ataxia

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MONDO:0014796 - autosomal recessive early-onset Parkinson disease 23

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MONDO:0011658 - autosomal recessive early-onset Parkinson disease 7

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MONDO:0013392 - autosomal recessive spinocerebellar ataxia 10

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MONDO:0014503 - autosomal recessive spinocerebellar ataxia 17

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MONDO:0008943 - autosomal recessive spinocerebellar ataxia 2

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MONDO:0014601 - autosomal recessive spinocerebellar ataxia 20

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MONDO:0980939 - basal ganglia calcification, idiopathic, 11, autosomal recessive

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MONDO:0014628 - basal ganglia calcification, idiopathic, 6

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MONDO:0008947 - bilateral striopallidodentate calcinosis

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MONDO:0979873 - brain small vessel disease 4

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MONDO:0980711 - brain small vessel disease 6 with leukoencephalopathy

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MONDO:0044720 - cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome

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MONDO:0014104 - cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 4

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MONDO:0013886 - cerebellar dysfunction with variable cognitive and behavioral abnormalities

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MONDO:0014862 - cerebral palsy, spastic quadriplegic, 3

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MONDO:0008083 - ceroid lipofuscinosis, neuronal, 4 (Kufs type)

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MONDO:0002797 - childhood medulloblastoma

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MONDO:0013541 - complex cortical dysplasia with other brain malformations 1

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MONDO:0014171 - complex cortical dysplasia with other brain malformations 4

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MONDO:0014337 - complex cortical dysplasia with other brain malformations 5

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MONDO:0014341 - complex cortical dysplasia with other brain malformations 6

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MONDO:0012399 - complex cortical dysplasia with other brain malformations 7

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MONDO:0011402 - congenital cataracts-facial dysmorphism-neuropathy syndrome

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MONDO:0009050 - Cushing disease due to pituitary adenoma

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MONDO:0030881 - developmental and epileptic encephalopathy 102

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MONDO:0031021 - developmental and epileptic encephalopathy 104

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MONDO:0031028 - developmental and epileptic encephalopathy 105 with hypopituitarism

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MONDO:0031055 - developmental and epileptic encephalopathy 107

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MONDO:0859325 - developmental and epileptic encephalopathy 109

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MONDO:0957780 - developmental and epileptic encephalopathy 111

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MONDO:0958330 - developmental and epileptic encephalopathy 113

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MONDO:0968946 - developmental and epileptic encephalopathy 115

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MONDO:0970945 - developmental and epileptic encephalopathy 116

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MONDO:0979238 - developmental and epileptic encephalopathy 118

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MONDO:0020630 - developmental and epileptic encephalopathy 91

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MONDO:0020632 - developmental and epileptic encephalopathy 93

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MONDO:0014150 - developmental and epileptic encephalopathy 94

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MONDO:0023659 - developmental and epileptic encephalopathy 96

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MONDO:0013389 - developmental and epileptic encephalopathy, 12

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MONDO:0014199 - developmental and epileptic encephalopathy, 17

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MONDO:0014392 - developmental and epileptic encephalopathy, 25

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MONDO:0014593 - developmental and epileptic encephalopathy, 29

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MONDO:0012245 - developmental and epileptic encephalopathy, 3

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MONDO:0014598 - developmental and epileptic encephalopathy, 31A

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MONDO:0957248 - developmental and epileptic encephalopathy, 31B

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MONDO:0014625 - developmental and epileptic encephalopathy, 33

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MONDO:0014719 - developmental and epileptic encephalopathy, 35

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MONDO:0010472 - developmental and epileptic encephalopathy, 36

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MONDO:0014868 - developmental and epileptic encephalopathy, 38

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MONDO:0012812 - developmental and epileptic encephalopathy, 4

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MONDO:0014895 - developmental and epileptic encephalopathy, 40

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MONDO:0014933 - developmental and epileptic encephalopathy, 44

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MONDO:0015000 - developmental and epileptic encephalopathy, 48

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MONDO:0014647 - developmental and epileptic encephalopathy, 50

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MONDO:0015025 - developmental and epileptic encephalopathy, 51

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MONDO:0033362 - developmental and epileptic encephalopathy, 53

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MONDO:0033364 - developmental and epileptic encephalopathy, 55

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MONDO:0033365 - developmental and epileptic encephalopathy, 56

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MONDO:0029138 - developmental and epileptic encephalopathy, 67

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MONDO:0034106 - developmental and epileptic encephalopathy, 73

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MONDO:0032752 - developmental and epileptic encephalopathy, 75

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MONDO:0032768 - developmental and epileptic encephalopathy, 76

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MONDO:0032808 - developmental and epileptic encephalopathy, 77

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MONDO:0032822 - developmental and epileptic encephalopathy, 80

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MONDO:0032858 - developmental and epileptic encephalopathy, 81

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MONDO:0032880 - developmental and epileptic encephalopathy, 82

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MONDO:0032895 - developmental and epileptic encephalopathy, 83

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MONDO:0026771 - developmental and epileptic encephalopathy, 85, with or without midline brain defects

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MONDO:0030059 - developmental and epileptic encephalopathy, 87

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MONDO:0005503 - developmental disorder of mental health

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MONDO:0006033 - diffuse intrinsic pontine glioma

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MONDO:0014233 - early-onset Parkinson disease 20

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Genes:

MONDO:0975801 - encephalopathy, acute transient

References:

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MONDO:0013726 - encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1

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MONDO:0005027 - epilepsy

References:

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MONDO:0015005 - epilepsy, early-onset, vitamin B6-dependent

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MONDO:0013322 - epilepsy, familial adult myoclonic, 3

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MONDO:0054846 - epilepsy, familial adult myoclonic, 6

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MONDO:0024556 - epilepsy, familial focal, with variable foci 1

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MONDO:0014924 - epilepsy, familial focal, with variable foci 2

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MONDO:0014925 - epilepsy, familial focal, with variable foci 3

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MONDO:0005384 - focal epilepsy

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MONDO:0100339 - Friedreich ataxia

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MONDO:0100340 - Friedreich ataxia 1

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MONDO:0014517 - generalized epilepsy with febrile seizures plus, type 9

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MONDO:0011612 - glycine encephalopathy

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MONDO:0958179 - glycine encephalopathy 1

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MONDO:0958192 - glycine encephalopathy 2

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MONDO:0018097 - infantile spasms

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MONDO:0044319 - intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies

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MONDO:0011818 - isolated focal cortical dysplasia type II

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MONDO:0011706 - Kufor-Rakeb syndrome

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MONDO:0008199 - late-onset Parkinson disease

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MONDO:0016532 - Lennox-Gastaut syndrome

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MONDO:0009567 - Marinesco-Sjogren syndrome

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MONDO:0007959 - medulloblastoma

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MONDO:0013254 - microcephaly, seizures, and developmental delay

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MONDO:0013542 - Moyamoya disease 5

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MONDO:0010466 - multiple congenital anomalies-hypotonia-seizures syndrome 2

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MONDO:0957382 - multiple mitochondrial dysfunctions syndrome 7

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MONDO:0958231 - neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism

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MONDO:0005180 - Parkinson disease

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MONDO:0013625 - Parkinson disease 17

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MONDO:0014742 - Parkinson disease 22, autosomal dominant

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MONDO:0957576 - Parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development

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MONDO:0030676 - parkinsonism-dystonia 3, childhood-onset

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MONDO:0013931 - peroxisome biogenesis disorder 4B

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MONDO:0008201 - Perry syndrome

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MONDO:0013526 - progressive myoclonic epilepsy type 6

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MONDO:0020074 - progressive myoclonus epilepsy

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MONDO:0012407 - pyridoxal phosphate-responsive seizures

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MONDO:0005090 - schizophrenia

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MONDO:0013498 - schizophrenia 15

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MONDO:0016163 - spinocerebellar ataxia 7

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MONDO:0011330 - spinocerebellar ataxia type 10

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MONDO:0011439 - spinocerebellar ataxia type 12

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MONDO:0011781 - spinocerebellar ataxia type 17

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MONDO:0008458 - spinocerebellar ataxia type 2

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MONDO:0012246 - spinocerebellar ataxia type 26

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MONDO:0012450 - spinocerebellar ataxia type 28

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MONDO:0007574 - spinocerebellar ataxia type 34

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MONDO:0013594 - spinocerebellar ataxia type 36

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MONDO:0014417 - spinocerebellar ataxia type 38

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MONDO:0014934 - spinocerebellar ataxia, autosomal recessive 24

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MONDO:0033115 - spinocerebellar ataxia, autosomal recessive 25

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MONDO:0032923 - spinocerebellar ataxia, autosomal recessive 28

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MONDO:0030312 - spinocerebellar ataxia, autosomal recessive 29

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MONDO:0030318 - spinocerebellar ataxia, autosomal recessive 30

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MONDO:0030323 - spinocerebellar ataxia, autosomal recessive 31

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MONDO:0011801 - spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1

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MONDO:0018996 - spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2

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MONDO:0018614 - undetermined early-onset epileptic encephalopathy

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MONDO:0010747 - X-linked dystonia-parkinsonism

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MONDO:0010547 - X-linked progressive cerebellar ataxia

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MONDO:0010524 - X-linked sideroblastic anemia with ataxia

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