DOPATREE
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DOPATREE
CONDITIONS
CONDITIONS / TYPES BY COMMON MEDICAL GROUPINGS
NEUROLOGY CONDITIONS-ALL (NEUROLOGICAL)
NEUROLOGY CONDITIONS / TYPES
MOVEMENT DISORDERS-ALL (MOTOR DISEASES, NEUROMUSCULAR, MUSCULAR, MUSCLE, MOTOR IMPAIRMENT)
MOVEMENT DISORDERS / LISTINGS
Parents
MOVEMENT DISORDERS-ALL (MOTOR DISEASES, NEUROMUSCULAR, MUSCULAR, MUSCLE, MOTOR IMPAIRMENT)
Children
ACTIN-ACCUMULATION MYOPATHY (ACTIN FILAMENT AGGREGATE MYOPATHY, ACTIN MYOPATHY, CONGENITAL MYOPATHY WITH EXCESS OF THIN FILAMENTS)
ADCY5-RELATED DYSKINESIA
AKATHISIA (RESTLESSNESS)
AMYOTROPHIC LATERAL SCLEROSIS (ALS, LOU GEHRIG'S DISEASE)
ATAXIA NEUROPATHY SPECTRUM (ANS, MIRAS, MITOCHONDRIAL RECESSIVE ATAXIA SYNDROME, SANDO, SENSORY ATAXIA NEUROPATHY DYSARTHRIA AND OPHTHALMOPLEGIA)
ATAXIA WITH VITAMIN E DEFICIENCY (AVED, FAMILIAL ISOLATED)
ATAXIA-ALL (SPINOCEREBELLAR ATAXIA, SCA)
ATAXIA-TELANGIECTASIA (A-T, ATAXIA TELANGIECTASIA SYNDROME, ATM, LOUIS-BAR SYNDROME, CEREBELLO-OCULOCUTANEOUS TELANGIECTASIA)
AUTOSOMAL DOMINANT HEREDITARY ATAXIA (EPISODIC ATAXIA, SPINOCEREBELLAR ATAXIA)
BECKER MUSCULAR DYSTROPHY (BMD, BENIGN JUVENILE MUSCULAR DYSTROPHY, BMD, PROGRESSIVE TARDIVE MUSCULAR DYSTROPHY)
BENIGN PAROXYSMAL POSITIONAL VERTIGO (BPPV, BENIGN POSITIONAL VERTIGO, VERTIGO - POSITIONAL, DIZZINESS - POSITIONAL)
CACHEXIA (CACHEXIC SYMPTOM)
CAV3-RELATED DISTAL MYOPATHY
CENTRAL CORE DISEASE (CCD, CENTRAL CORE MYOPATHY, SHY-MAGEE SYNDROME, CCO, MUSCLE CORE DISEASE, MUSCULAR)
CENTRONUCLEAR MYOPATHY (CNM)
CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY (AUTOSOMAL DOMINANT, ADCADN)
CEREBRAL PALSY (CP, INFANTILE CEREBRAL PARALYSIS, LITTLE DISEASE, DIPLEGIA)
CERVICAL DYSTONIA (SPASMODIC TORTICOLLIS, ST, WRYNECK)
CONGENITAL HYPOMYELINATION NEUROPATHY (CHN, CHARCOT-MARIE-TOOTH TYPE 4E, CMT4E, CONGENITAL DYSMYELINATING NEUROPATHY, POLYNEUROPATHY)
CONGENITAL MUSCULAR DYSTROPHY (CMD)
CONGENITAL MUSCULAR DYSTROPHY, LMNA-RELATED (LMNA-RELATED CONGENITAL MUSCULAR DYSTROPHY, L-CMD, MDCL)
CONGENITAL MYASTHENIC SYNDROME (CMS, CONGENITAL MYASTHENIA)
CONGENITAL MYOPATHY (CENTRAL CORE DISEASE, CENTRONUCULEAR MYOPATHY, NEMALINE, BATTEN TURNER CONGENITAL MYOPATHY)
DEJERINE-SOTTAS SYNDROME (DSS, NEUROPATHY, PROGRESSIVE HYPERTROPHIC INTERSTITIAL POLYNEUROPATHY OF CHILDHOOD, ONION BULB NEUROPATHY, CHARCOT-MARIE-TOOTH DISEASE, TYPE 3, CMT3)
DISTAL MYOPATHY (DISTAL MUSCULAR DYSTROPHY, DMD, DM, MIYOSHI, VCP, WELANDER, LAING, GNE, NONAKA, HERDITARY INCLUSION-BODY MYOPATHY, MARKESBERY-GRIGGS, MIYOSHI MUSCULAR DYSTROPHY, MMD)
DUCHENNE MUSCULAR DYSTROPHY (DMD GENE, X-LINKED RECESSIVE, DYSTROPHIN, PSEUDOHYPERTROPHIC PROGRESSIVE, DUCHENNE TYPE, NONSENSE MUTATION DYSTROPHINOPATHY, NMDBMD, DUCHENNE'S)
DYSKINESIA (INVOLUNTARY MUSCLE MOVEMENTS, SYMPTOM)
DYSPRAXIA (DEVELOPMENTAL, DEVELOPMENTAL COORDINATION DISORDER, DEVELOPMENTAL MOTOR COORDINATION DISORDER)
DYSTONIA (PRIMARY, ALL, GENERALIZED, SEGMENTAL, MULTIFOCAL, MULTI-FOCAL, EARLY-ONSET PRIMARY DYSTONIA, TASK-SPECIFIC)
DYSTONIA 6 (DYT6, IDIOPATHIC TORSION DYSTONIA OF MIXED TYPE, THAP1 DYSTONIA)
DYSTROPHINOPATHY (DYSTROPHINOPATHIES)
EMERY-DREIFUSS MUSCULAR DYSTROPHY (EDMD, EMERY DREIFUSS)
ENDOCRINE MYOPATHY (THYROTOXIC MYOPATHY, HYPERTHYROID, HYPOTHYROID MYOPATHY)
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY (FSH, FSHD, FMD, FACIO-SCAPULO-HUMERAL DYSTROPHY)
FIBROUS DYSPLASIA OF BONE (FD, CONNECTIVE TISSUE, JAFFE-LICHTENSTEIN DISEASE)
FOCAL HAND DYSTONIA (FHD, MOGIGRAPHIA AND SCRIVENER'S PALSY, WRITER'S CRAMP, LIMB DYSTONIA)
FRAGILE X-ASSOCIATED TREMOR/ATAXIA SYNDROME
FRAILTY SYNDROME
FRIEDREICH ATAXIA (FRIEDREICH'S ATAXIA, SPINOCEREBELLAR ATAXIA, FRIEDREICH, HEREDITARY SPINAL SCLEROSIS, FRDA)
GNE MYOPATHY (HEREDITARY INCLUSION BODY MYOPATHY, HIBM, IBM2, QSM, DMRV, NONAKA, RIMMED VACUOLE, QUADRICEPS SPARING, INCLUSION BODY MYOPATHY 2)
HIKER'S FEET (HYPERKERATOSIS, TOES, PLANTAR FEET)
ICU ACQUIRED WEAKNESS (ICUAW)
INFLAMMATORY MYOPATHY (MYOPATHIES)
ION CHANNEL DISEASES (CHANNELOPATHY)
JUVENILE MYOSITIS (JM, JUVENILE DERMATOMYOSITIS, JDM, JUVENILE POLYMYOSITIS, JPM)
KEARNS-SAYRE SYNDROME (KSS, OCULOCRANIOSOMATIC SYNDROME, CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA AND MYOPATHY, KEARNS-SAYRE MITOCHONDRIAL CYTOPATHY)
KENNEDY DISEASE (SPINAL AND BULBAR MUSCULAR ATROPHY, SPINAL-BULBAR, SBMA, KD, X-LINKED, SPINOBULBAR MUSCULAR ATROPHY)
KUFOR RAKEB SYNDROME (KRS, AUTOSOMAL RECESSIVE, JUVENILE ONSET PARKINSON’S DISEASE 9, PARKINSON’S DISEASE 9)
LAMBERT-EATON MYASTHENIC SYNDROME (LEMS)
LEIGH SYNDROME (SUBACUTE NECROTIZING ENCEPHALOMYOPATHY, SNE, MATERNALLY INHERITED LEIGH SYNDROME, MILS)
LIMB-GIRDLE MUSCULAR DYSTROPHY (LGMD, ERB'S, PELVOFEMORAL MUSCULAR DYSTROPHY, PROXIMAL MUSCULAR DYSTROPHY)
LOCKED IN SYNDROME (LOCKED-IN, LOCKEDIN, CEREBROMEDULLOSPINAL DISCONNECTION, DE-EFFERENTED STATE, PSEUDOCOMA)
MITOCHONDRIAL CONDITIONS-ALL (PRIMARY MITOCHONDRIAL DISEASE, PMD)
MITOCHONDRIAL DNA DEPLETION SYNDROME (MDS)
MITOCHONDRIAL ENCEPHALOMYOPATHY LACTIC ACIDOSIS AND STROKE-LIKE EPISODES (MELAS SYNDROME)
MITOCHONDRIAL MYOPATHY (MM, MYOPATHIES, PMM, PRIMARY)
MOTION SICKNESS (CAR SICK, SEA SICK, AIR SICK)
MOTOR NEURON DISEASE (MND)
MULTIFOCAL MOTOR NEUROPATHY (MMN, MMNCB, CONDUCTION BLOCK)
MUSCULAR ATROPHY (SYMPTOM)
MUSCULAR DYSTROPHY-ALL
MYASTHENIA GRAVIS (MG)
MYOCLONIC EPILEPSY WITH RAGGED RED FIBERS (MERRF, FUKUHARA SYNDROME)
MYOCLONUS (INVOLUNTARY JERKING OF MUSCLES, SYMPTOM, ALL)
MYOPATHY (MYOFIBRILLAR)
MYOPATHY (MYOPATHIES)
MYOSITIS (ALL, SPORADIC INCLUSION BODY MYOSITIS, SIBM, INCLUSION BODY MYOSITIS, IBM)
MYOTONIA CONGENITA (THOMSEN DISEASE AND BECKER TYPE)
MYOTONIC DYSTROPHY (DYSTROPHIA MYOTONICA, CURSCHMANN-BATTEN-STEINERT SYNDROME, DM, MYOTONIA ATROPHICA, STEINERT DISEASE, MYOTONIC MUSCULAR DYSTROPHY, PROXIMAL MYOTONIC MYOPATHY, PROMM)
NEMALINE MYOPATHY (NM, ROD BODY DISEASE, TYPICAL CONGENITAL NEMALINE MYOPATHY)
NEUROMUSCULAR JUNCTION DISEASE (NJD, NMJD)
NEUROPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE (MOTOR NEUROPATHY DISTAL JERASH TYPE, MNDJ, SPINAL MUSCULAR ATROPHY JERASH TYPE)
NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE II
NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE V (DHMN-V, DISTAL HEREDITARY MOTOR NEURONOPATHY TYPE 5)
OCULOPHARYNGEAL MUSCULAR DYSTROPHY (OPMD, OCULOPHARYNGODISTAL MYOPATHY)
PARAMYOTONIA CONGENITA (PC, EULENBURG DISEASE, PARALYSIS PERIODICA PARAMYOTONICA, PMC, VON EULENBURG'S DISEASE)
PARKINSON'S DISEASE (PD, SNCA, PARK1, UCHL1, PARK5, LRRK2, PARK8, PARK3, PARK2, PARK7 GENES, PARKINSONISM)
PERIODIC LIMB MOVEMENT DISORDER (PLMD)
POST-POLIO SYNDROME (POST POLIO SYNDROME, PPS, POLIOMYELITIS SEQUELAE)
PRIMARY ORTHOSTATIC TREMOR (POT, IDIOPATHIC ORTHOSTATIC TREMOR, IOT, STANDING)
RESTLESS LEG SYNDROME (RLS, WILLIS EKBOM DISEASE)
RHABDOMYOLYSIS
RHYTHMIC MOVEMENT DISORDER (RMD)
RIGID SPINE SYNDROME (RSS, RIGID SPINE MUSCULAR DYSTROPHY-1, RSMD1)
RYR1-RELATED DISEASES (MYOPATHY, MUSCLE DISEASE)
SARCOPENIA
SCAPULOPERONEAL MUSCULAR DYSTROPHY (SPMD, SMD)
SPASTICITY (UPPER LIMB, LOWER LIMB, POST-STROKE)
SPINA BIFIDA (SPINAL DYSRAPHISM, CLEFT SPINE, OPEN SPINE, NEURAL TUBE DEFECT, SB, SPINA BIFIDA OCCULTA, SBO)
SPINAL CORD INJURY (SCI, PARAPLEGIA, TETRAPLEGIA)
SPINAL MUSCULAR ATROPHY WITH LOWER EXTREMITY PREDOMINANCE (SMA-LED, KUGELBERG WELANDER SYNDROME, KWS, SMA3, SPINAL MUSCULAR ATROPHY TYPE 3)
SPINAL MUSCULAR ATROPHY-ALL (SMA, RESPIRATORY DISTRESS, DIAPHRAGMATIC, DISTAL, RESPIRATORY FAILURE, WERDNIG-HOFFMAN DISEASE, DUBOWITZ DISEASE, KUGELBERG-WELANDER DISEASE, JUVENILE)
SPINAL MUSCULAR ATROPHY-PROGRESSIVE MYOCLONIC EPILEPSY SYNDROME (SMA-PME, HEREDITARY MYOCLONUS-PROGRESSIVE DISTAL MUSCULAR ATROPHY SYNDROME, JANKOVIC–RIVERA SYNDROME)
SPINOCEREBELLAR ATAXIA (SCA, SPINOCEREBELLAR ATROPHY, DEGENERATION, ALL, GENERAL)
SPINOCEREBELLAR ATAXIA 1 (SCA1, SPINOCEREBELLAR ATAXIA TYPE 1, OLIVOPONTOCEREBELLAR ATROPHY 1)
SPINOCEREBELLAR ATAXIA 10 (SCA10, TYPE 10)
SPINOCEREBELLAR ATAXIA 11 (SCA11, TYPE 11)
SPINOCEREBELLAR ATAXIA 12 (SCA12, TYPE 12)
SPINOCEREBELLAR ATAXIA 13 (SCA13, TYPE 13)
SPINOCEREBELLAR ATAXIA 14 (SCA14, TYPE 14)
SPINOCEREBELLAR ATAXIA 15 (SCA15, TYPE 15)
SPINOCEREBELLAR ATAXIA 17 (SCA17, TYPE 17)
SPINOCEREBELLAR ATAXIA 18 (SCA18, TYPE 18)
SPINOCEREBELLAR ATAXIA 19 AND 22 (SCA19, SCA22, TYPE 19, TYPE 22)
SPINOCEREBELLAR ATAXIA 2 (SCA2, TYPE 2)
SPINOCEREBELLAR ATAXIA 20 (SCA20, TYPE 20)
SPINOCEREBELLAR ATAXIA 21 (SCA21, TYPE 21)
SPINOCEREBELLAR ATAXIA 23 (SCA23, TYPE 23)
SPINOCEREBELLAR ATAXIA 25 (SCA25, TYPE 25)
SPINOCEREBELLAR ATAXIA 26 (SCA26, TYPE 26)
SPINOCEREBELLAR ATAXIA 27 (SCA27, TYPE 27)
SPINOCEREBELLAR ATAXIA 28 (SCA28, TYPE 28)
SPINOCEREBELLAR ATAXIA 29 (SCA29, TYPE 29)
SPINOCEREBELLAR ATAXIA 3 (SCA3, TYPE 3, AZOREAN ATAXIA, AZOREAN DISEASE, MACHADO-JOSEPH DISEASE, MJD)
SPINOCEREBELLAR ATAXIA 30 (SCA30, TYPE 30)
SPINOCEREBELLAR ATAXIA 31 (SCA31, TYPE 31, 16Q22-LINKED)
SPINOCEREBELLAR ATAXIA 34 (SCA34, TYPE 34, GIROUX BARBEAU SYNDROME, ERYTHROKERATODERMIA - ATAXIA)
SPINOCEREBELLAR ATAXIA 36 (ASIDAN ATAXIA, COSTA DE MORTE ATAXIA, SCA36, TYPE 36)
SPINOCEREBELLAR ATAXIA 4 (SCA4, TYPE 4)
SPINOCEREBELLAR ATAXIA 5 (SCA5, TYPE 5)
SPINOCEREBELLAR ATAXIA 6 (SCA6, TYPE 6)
SPINOCEREBELLAR ATAXIA 7 (SCA7, TYPE 7)
SPINOCEREBELLAR ATAXIA 8 (SCA8, TYPE 8)
SPINOCEREBELLAR ATAXIA 9 (SCA9, TYPE 9)
SPINOCEREBELLAR ATAXIA AUTOSOMAL RECESSIVE 3 (SCAR3, SPINOCEREBELLAR ATAXIA WITH BLINDNESS AND DEAFNESS, AUTOSOMAL RECESSIVE CEREBELLAR ATAXIA - BLINDNESS - DEAFNESS)
SPINOCEREBELLAR ATAXIA AUTOSOMAL RECESSIVE 4 (SCAR4, SPINOCEREBELLAR ATAXIA WITH SACCADIC INTRUSIONS, SCASI)
SPINOCEREBELLAR ATAXIA AUTOSOMAL RECESSIVE 5 (SCAR5, CAMOS)
SPINOCEREBELLAR ATAXIA AUTOSOMAL RECESSIVE 6 (SCAR6, CEREBELLAR ATAXIA INFANTILE NONPROGRESSIVE AUTOSOMAL RECESSIVE, NORWEGIAN INFANTILE ONSET ATAXIA)
SPINOCEREBELLAR ATAXIA AUTOSOMAL RECESSIVE 7 (SCAR7, CHILDHOOD ONSET AUTOSOMAL RECESSIVE SLOWLY PROGRESSIVE SPINOCEREBELLAR ATAXIA)
SPINOCEREBELLAR ATAXIA AUTOSOMAL RECESSIVE 8 (ARCA1, SCAR8)
SPINOCEREBELLAR ATAXIA WITH AXONAL NEUROPATHY TYPE 1 (SCAN1, AUTOSOMAL RECESSIVE)
SPINOCEREBELLAR ATAXIA WITH DYSMORPHISM
SPINOCEREBELLAR ATAXIA X-LINKED TYPE 2 (SCAX2, CEREBELLAR ATAXIA WITH EXTRAPYRAMIDAL INVOLVEMENT EARLY-ONSET)
SPINOCEREBELLAR ATAXIA X-LINKED TYPE 3 (SCAX3, ATAXIA-DEAFNESS SYNDROME X-LINKED)
SPINOCEREBELLAR ATAXIA X-LINKED TYPE 4 (SCAX4, ATAXIA-DEMENTIA SYNDROME X-LINKED)
SPINOCEREBELLAR DEGENERATION AND CORNEAL DYSTROPHY (CORNEAL CEREBELLAR SYNDROME, DER KALOUSTIAN JARUDI KHOURY SYNDROME)
STEREOTYPIC MOVEMENT DISORDER (SMD)
TOURETTE SYNDROME (TIC DISORDER, CHRONIC MOTOR AND VOCAL TIC DISORDER, GILLES DE LA TOURETTE SYNDROME, TD, TOURETTE DISORDER)
TREMOR (ESSENTIAL, FAMILIAL, HEREDITARY)
ULLRICH CONGENITAL MUSCULAR DYSTROPHY (UCMD, ULLRICH DISEASE, ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY)
VESTIBULAR NEURITIS (LABYRINTHITIS)
WORSTER DROUGHT SYNDROME (WDS)
X-LINKED DYSTONIA-PARKINSONISM (LUBAG SYNDROME, DYT3, DYSTONIA-PARKINSONISM, X-LINKED, XDP, X-LINKED DYSTONIA OF PANAY)
X-LINKED INFANTILE SPINAL MUSCULAR ATROPHY (XLSMA, XL-SMA, SMAX2, AMCX1, ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED)