Table 2 Open in new tab The NDs labels...

Disease label

Disease name

UniProt

Disease Ontology

MESH

Multiple Sclerosis

DI-02604

DOID:2377

MESH:D009103

CPM

Central Pontine Myelinolysis

N/A

DOID:636

MESH:D017590

OPCA

Olivopontocerebellar Atrophy

N/A

DOID:14784

MESH:D009849

XLHAX

X-linked Hereditary Ataxia

N/A

DOID:0050953

N/A

PCD

Primary Cerebellar Degeneration

N/A

DOID:9277

MESH:D013132

PXP

Plexopathy

N/A

DOID:3688

N/A

PBP

Progressive Bulbar Palsy

N/A

DOID:681

MESH:D010244

Lateral Sclerosis

N/A

DOID:230

MESH:D016472

CAR

Autosomal Recessive Cerebellar Ataxia

DI-01061

DOID:0050950

N/A

Alzheimer Disease

DI-03832

DOID:10652

MESH:D000544

Huntington Disease

DI-01754

DOID:12858

MESH:D006816

LFD

Lafora Disease

N/A

DOID:3534

MESH:D020192

SPOAN

SPOAN Syndrome

N/A

DOID:0060491

MESH:C563702

ICRD

Infantile Cerebellar–Retinal Degeneration

DI-03409

DOID:0050883

N/A

MCD

Myoclonic Cerebellar Dyssynergia

N/A

DOID:12707

MESH:D002527

ACCPN

Agenesis of the Corpus Callosum with Peripheral Neuropathy

DI-00054

DOID:0090003

N/A

PMA

Progressive Muscular Atrophy

N/A

DOID:318

MESH:D009134

SPAX

Spastic Ataxia

DI-04137

DOID:0050952

N/A

Parkinson Disease

DI-02134

DOID:14330

MESH:D010300

Motor Neuritis

N/A

DOID:683

MESH:D009443

PIDB

Pick Disease

DI-02937

DOID:11870

MESH:D020774

BCS

Balo Concentric Sclerosis

N/A

DOID:0060215

MESH:D002549

CHAC

Choreaacanthocytosis

DI-01344

DOID:0050766

MESH:D054546

PPD

Postencephalitic Parkinson Disease

N/A

DOID:14332

MESH:D010301

FENIB

Familial Encephalopathy with Neuroserpin Inclusion Bodies

DI-01567

DOID:0050831

MESH:C536841

ASD

Autism Spectrum Disorder

N/A

DOID:0060041

MESH:D000067877

ALS

Amyotrophic Lateral Sclerosis

DI-00107

DOID:332

MESH:D000690

ADCA

Autosomal Dominant Cerebellar Ataxia

DI-03793

DOID:1441

MESH:D020754

SMA

Spinal Muscular Atrophy

DI-01055

DOID:12377

MESH:D009134

PSNP1

Pseudobulbar Palsy

DI-02215

DOID:12680

MESH:D020828

Episodic Ataxia

DI-00475

DOID:963

MESH:C580065

DLB

Lewy Body Dementia

DI-01901

DOID:12217

MESH:D020961

PCH

Pontocerebellar Hypoplasia

DI-02626

DOID:0060264

MESH:C580383

MSA

Multiple System Atrophy

DI-03867

DOID:4752

MESH:D012791, MESH:D019578

NBIA1

Pantothenate Kinase-associated Neurodegeneration

DI-02126

DOID:3981

MESH:D006211

Table 2

Open in new tab

The NDs labels and cross-reference links in NDAtlas

Disease label	Disease name	UniProt	Disease Ontology	MESH
MS	Multiple Sclerosis	DI-02604	DOID:2377	MESH:D009103
CPM	Central Pontine Myelinolysis	N/A	DOID:636	MESH:D017590
OPCA	Olivopontocerebellar Atrophy	N/A	DOID:14784	MESH:D009849
XLHAX	X-linked Hereditary Ataxia	N/A	DOID:0050953	N/A
PCD	Primary Cerebellar Degeneration	N/A	DOID:9277	MESH:D013132
PXP	Plexopathy	N/A	DOID:3688	N/A
PBP	Progressive Bulbar Palsy	N/A	DOID:681	MESH:D010244
LS	Lateral Sclerosis	N/A	DOID:230	MESH:D016472
CAR	Autosomal Recessive Cerebellar Ataxia	DI-01061	DOID:0050950	N/A
AD	Alzheimer Disease	DI-03832	DOID:10652	MESH:D000544
HD	Huntington Disease	DI-01754	DOID:12858	MESH:D006816
LFD	Lafora Disease	N/A	DOID:3534	MESH:D020192
SPOAN	SPOAN Syndrome	N/A	DOID:0060491	MESH:C563702
ICRD	Infantile Cerebellar–Retinal Degeneration	DI-03409	DOID:0050883	N/A
MCD	Myoclonic Cerebellar Dyssynergia	N/A	DOID:12707	MESH:D002527
ACCPN	Agenesis of the Corpus Callosum with Peripheral Neuropathy	DI-00054	DOID:0090003	N/A
PMA	Progressive Muscular Atrophy	N/A	DOID:318	MESH:D009134
SPAX	Spastic Ataxia	DI-04137	DOID:0050952	N/A
PD	Parkinson Disease	DI-02134	DOID:14330	MESH:D010300
MN	Motor Neuritis	N/A	DOID:683	MESH:D009443
PIDB	Pick Disease	DI-02937	DOID:11870	MESH:D020774
BCS	Balo Concentric Sclerosis	N/A	DOID:0060215	MESH:D002549
CHAC	Choreaacanthocytosis	DI-01344	DOID:0050766	MESH:D054546
PPD	Postencephalitic Parkinson Disease	N/A	DOID:14332	MESH:D010301
FENIB	Familial Encephalopathy with Neuroserpin Inclusion Bodies	DI-01567	DOID:0050831	MESH:C536841
ASD	Autism Spectrum Disorder	N/A	DOID:0060041	MESH:D000067877
ALS	Amyotrophic Lateral Sclerosis	DI-00107	DOID:332	MESH:D000690
ADCA	Autosomal Dominant Cerebellar Ataxia	DI-03793	DOID:1441	MESH:D020754
SMA	Spinal Muscular Atrophy	DI-01055	DOID:12377	MESH:D009134
PSNP1	Pseudobulbar Palsy	DI-02215	DOID:12680	MESH:D020828
EA	Episodic Ataxia	DI-00475	DOID:963	MESH:C580065
DLB	Lewy Body Dementia	DI-01901	DOID:12217	MESH:D020961
PCH	Pontocerebellar Hypoplasia	DI-02626	DOID:0060264	MESH:C580383
MSA	Multiple System Atrophy	DI-03867	DOID:4752	MESH:D012791, MESH:D019578
NBIA1	Pantothenate Kinase-associated Neurodegeneration	DI-02126	DOID:3981	MESH:D006211

Disease label	Disease name	UniProt	Disease Ontology	MESH
MS	Multiple Sclerosis	DI-02604	DOID:2377	MESH:D009103
CPM	Central Pontine Myelinolysis	N/A	DOID:636	MESH:D017590
OPCA	Olivopontocerebellar Atrophy	N/A	DOID:14784	MESH:D009849
XLHAX	X-linked Hereditary Ataxia	N/A	DOID:0050953	N/A
PCD	Primary Cerebellar Degeneration	N/A	DOID:9277	MESH:D013132
PXP	Plexopathy	N/A	DOID:3688	N/A
PBP	Progressive Bulbar Palsy	N/A	DOID:681	MESH:D010244
LS	Lateral Sclerosis	N/A	DOID:230	MESH:D016472
CAR	Autosomal Recessive Cerebellar Ataxia	DI-01061	DOID:0050950	N/A
AD	Alzheimer Disease	DI-03832	DOID:10652	MESH:D000544
HD	Huntington Disease	DI-01754	DOID:12858	MESH:D006816
LFD	Lafora Disease	N/A	DOID:3534	MESH:D020192
SPOAN	SPOAN Syndrome	N/A	DOID:0060491	MESH:C563702
ICRD	Infantile Cerebellar–Retinal Degeneration	DI-03409	DOID:0050883	N/A
MCD	Myoclonic Cerebellar Dyssynergia	N/A	DOID:12707	MESH:D002527
ACCPN	Agenesis of the Corpus Callosum with Peripheral Neuropathy	DI-00054	DOID:0090003	N/A
PMA	Progressive Muscular Atrophy	N/A	DOID:318	MESH:D009134
SPAX	Spastic Ataxia	DI-04137	DOID:0050952	N/A
PD	Parkinson Disease	DI-02134	DOID:14330	MESH:D010300
MN	Motor Neuritis	N/A	DOID:683	MESH:D009443
PIDB	Pick Disease	DI-02937	DOID:11870	MESH:D020774
BCS	Balo Concentric Sclerosis	N/A	DOID:0060215	MESH:D002549
CHAC	Choreaacanthocytosis	DI-01344	DOID:0050766	MESH:D054546
PPD	Postencephalitic Parkinson Disease	N/A	DOID:14332	MESH:D010301
FENIB	Familial Encephalopathy with Neuroserpin Inclusion Bodies	DI-01567	DOID:0050831	MESH:C536841
ASD	Autism Spectrum Disorder	N/A	DOID:0060041	MESH:D000067877
ALS	Amyotrophic Lateral Sclerosis	DI-00107	DOID:332	MESH:D000690
ADCA	Autosomal Dominant Cerebellar Ataxia	DI-03793	DOID:1441	MESH:D020754
SMA	Spinal Muscular Atrophy	DI-01055	DOID:12377	MESH:D009134
PSNP1	Pseudobulbar Palsy	DI-02215	DOID:12680	MESH:D020828
EA	Episodic Ataxia	DI-00475	DOID:963	MESH:C580065
DLB	Lewy Body Dementia	DI-01901	DOID:12217	MESH:D020961
PCH	Pontocerebellar Hypoplasia	DI-02626	DOID:0060264	MESH:C580383
MSA	Multiple System Atrophy	DI-03867	DOID:4752	MESH:D012791, MESH:D019578
NBIA1	Pantothenate Kinase-associated Neurodegeneration	DI-02126	DOID:3981	MESH:D006211

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