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Term:
neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language (DOID:0070050)
Annotations: Rat: (1) Mouse: (2) Human: (5) Chinchilla: (1) Bonobo: (1) Dog: (2) Squirrel: (1) Pig: (2) Naked Mole-rat: (1) Green Monkey: (1)
Parent Terms Term With Siblings Child Terms
3-M syndrome +   
AGAT deficiency  
AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency  
Al-Raqad Syndrome  
Alazami-Yuan Syndrome  
Alcohol Withdrawal Seizures  
Allan-Herndon-Dudley syndrome  
Alopecia, Epilepsy, Pyorrhea, Mental Subnormality 
Alopecia-Epilepsy-Oligophrenia Syndrome of Moynahan 
Arboleda-Tham syndrome  
Arthrogryposis Epileptic Seizures Migrational Brain Disorder 
Arthrogryposis, Impaired Intellectual Development, and Seizures  
articulation disorder +   
ATAXIA, INTENTION TREMOR, AND HYPOTONIA SYNDROME, CHILDHOOD-ONSET  
ATAXIA, PROGRESSIVE SEIZURES, MENTAL DETERIORATION, AND HEARING LOSS  
Atonic-Astatic Syndrome of Foerster 
Au-Kline Syndrome  
autoimmune epilepsy 
autosomal dominant intellectual developmental disorder 1  
autosomal dominant intellectual developmental disorder 10  
autosomal dominant intellectual developmental disorder 11  
autosomal dominant intellectual developmental disorder 13  
autosomal dominant intellectual developmental disorder 19  
autosomal dominant intellectual developmental disorder 2  
autosomal dominant intellectual developmental disorder 21  
autosomal dominant intellectual developmental disorder 22  
autosomal dominant intellectual developmental disorder 23  
autosomal dominant intellectual developmental disorder 26  
autosomal dominant intellectual developmental disorder 29  
autosomal dominant intellectual developmental disorder 3  
autosomal dominant intellectual developmental disorder 30  
autosomal dominant intellectual developmental disorder 31  
autosomal dominant intellectual developmental disorder 33  
autosomal dominant intellectual developmental disorder 34  
autosomal dominant intellectual developmental disorder 35  
autosomal dominant intellectual developmental disorder 36  
autosomal dominant intellectual developmental disorder 38  
autosomal dominant intellectual developmental disorder 39  
autosomal dominant intellectual developmental disorder 4  
autosomal dominant intellectual developmental disorder 40  
autosomal dominant intellectual developmental disorder 41  
autosomal dominant intellectual developmental disorder 42  
autosomal dominant intellectual developmental disorder 43  
autosomal dominant intellectual developmental disorder 44  
autosomal dominant intellectual developmental disorder 45  
autosomal dominant intellectual developmental disorder 46  
autosomal dominant intellectual developmental disorder 47  
autosomal dominant intellectual developmental disorder 48  
autosomal dominant intellectual developmental disorder 5  
autosomal dominant intellectual developmental disorder 50  
autosomal dominant intellectual developmental disorder 51  
autosomal dominant intellectual developmental disorder 52  
autosomal dominant intellectual developmental disorder 53  
autosomal dominant intellectual developmental disorder 54  
autosomal dominant intellectual developmental disorder 55  
autosomal dominant intellectual developmental disorder 56  
autosomal dominant intellectual developmental disorder 57  
autosomal dominant intellectual developmental disorder 58  
autosomal dominant intellectual developmental disorder 59  
autosomal dominant intellectual developmental disorder 6  
autosomal dominant intellectual developmental disorder 60 with seizures  
autosomal dominant intellectual developmental disorder 61  
autosomal dominant intellectual developmental disorder 62  
autosomal dominant intellectual developmental disorder 63 with macrocephaly  
autosomal dominant intellectual developmental disorder 64  
autosomal dominant intellectual developmental disorder 65  
autosomal dominant intellectual developmental disorder 66  
autosomal dominant intellectual developmental disorder 67  
autosomal dominant intellectual developmental disorder 68  
autosomal dominant intellectual developmental disorder 69  
autosomal dominant intellectual developmental disorder 7  
autosomal dominant intellectual developmental disorder 70  
autosomal dominant intellectual developmental disorder 71 with behavioral abnormalities  
autosomal dominant intellectual developmental disorder 72  
autosomal dominant intellectual developmental disorder 73  
autosomal dominant intellectual developmental disorder 74  
autosomal dominant intellectual developmental disorder 75  
autosomal dominant intellectual developmental disorder 8  
autosomal dominant intellectual developmental disorder type FRA12A  
autosomal recessive intellectual developmental disorder 73  
autosomal recessive spinocerebellar ataxia 12  
Baraitser-Winter syndrome +   
Battaglia Neri Syndrome 
Beta-Amino Acids, Renal Transport of 
Birk-Barel syndrome  
Borjeson-Forssman-Lehmann syndrome  
Boudhina Yedes Khiari syndrome 
branched-chain keto acid dehydrogenase kinase deficiency  
BRUNET-WAGNER NEURODEVELOPMENTAL SYNDROME  
Bryant-Li-Bhoj neurodevelopmental syndrome +   
Carnitine Acetyltransferase Deficiency  
Cerebellar Atrophy with Seizures and Variable Developmental Delay  
CEREBELLAR ATROPHY, DEVELOPMENTAL DELAY, AND SEIZURES  
Christianson syndrome  
chromosome 17p13.1 deletion syndrome 
Chromosome 7q11.23 Deletion Syndrome, Distal, 1.2-MB  
Clark-Baraitser syndrome  
Coffin Syndrome 1 
Coffin-Siris syndrome +   
Coffin-Siris syndrome 9  
Cohen syndrome  
combined oxidative phosphorylation deficiency 3  
Congenital Hypotonia, Epilepsy, Developmental Delay, and Digital Anomalies  
congenital limbs-face contractures-hypotonia-developmental delay syndrome  
De Hauwere syndrome  
Der Kaloustian Mcintosh Silver Syndrome 
DeSanto-Shinawi syndrome  
developmental delay and seizures with or without movement abnormalities  
Developmental Delay with Hypotonia, Myopathy, and Brain Abnormalities  
DEVELOPMENTAL DELAY WITH OR WITHOUT EPILEPSY  
developmental delay, dysmorphic facies, and brain anomalies  
Developmental Delay, Epilepsy, and Neonatal Diabetes  
developmental delay, hypotonia, and impaired language  
DEVELOPMENTAL DELAY, HYPOTONIA, MUSCULOSKELETAL DEFECTS, AND BEHAVIORAL ABNORMALITIES  
DEVELOPMENTAL DELAY, IMPAIRED SPEECH, AND BEHAVIORAL ABNORMALITIES  
DEVELOPMENTAL DELAY, IMPAIRED SPEECH, AND BEHAVIORAL ABNORMALITIES, WITH OR WITHOUT SEIZURES  
Diencephalic-Mesencephalic Junction Dysplasia Syndrome 2  
Drug Resistant Epilepsy +   
Dyskinesias, Seizures, and Intellectual Developmental Disorder  
early-onset epilepsy 2  
early-onset epilepsy 3  
echolalia 
electroclinical syndrome +   
Emanuel Syndrome 
Epilepsy Telangiectasia 
Epilepsy, Occipital Calcifications 
Ethanolaminosis 
Experimental Seizures  
extratemporal epilepsy 
Facial Dysmorphism, Hypertrichosis, Epilepsy, Intellectual/Developmental Delay, and Gingival Overgrowth Syndrome  
Febrile Seizures +   
FERGUSON-BONNI NEURODEVELOPMENTAL SYNDROME  
FG syndrome +   
Focal Cortical Dysplasia of Taylor +   
focal epilepsy +   
Focal Epilepsy with Speech Disorder and with or without Mental Retardation  
fumarase deficiency  
GAND syndrome  
generalized epilepsy +   
German Syndrome 
GLOBAL DEVELOPMENTAL DELAY WITH SPEECH AND BEHAVIORAL ABNORMALITIES  
glycogen storage disease IX +   
Glycosylphosphatidylinositol Biosynthesis Defect 25  
Glycosylphosphatidylinositol Deficiency +   
GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY  
Grubben de Cock Borghgraef Syndrome 
Gurrieri Sammito Bellussi Syndrome 
Halperin-Birk syndrome  
Helsmoortel-Van Der Aa syndrome  
Houge-Janssens Syndrome +   
Hyperglycinemia, Lactic Acidosis, and Seizures  
Hyperphosphatemia, Polyuria, and Seizures 
HYPOMAGNESEMIA, SEIZURES, AND INTELLECTUAL DISABILITY +   
hypotonia, ataxia, and delayed development syndrome  
HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME  
Hypotonia, Congenital Nystagmus, Ataxia and Abnormal Auditory Brainstem Response 
Hypotonia, Seizures, and Precocious Puberty 
hypotonia-cystinuria syndrome  
Infantile Hypotonia with Psychomotor Retardation +   
Infra-Auricular Cutaneous Creases with Tall Stature and Advanced Bone Age 
intellectual developmental disorder with autistic features and language delay, with or without seizures  
Intellectual Developmental Disorder with Behavioral Abnormalities and Craniofacial Dysmorphism with or without Seizures  
Intellectual Developmental Disorder with Dysmorphic Facies, Seizures, and Distal Limb Anomalies  
INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPOTONIA AND BEHAVIORAL ABNORMALITIES  
intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies  
Intellectual Developmental Disorder with Macrocephaly, Seizures, and Speech Delay  
INTELLECTUAL DEVELOPMENTAL DISORDER WITH POLYMICROGYRIA AND SEIZURES  
INTELLECTUAL DEVELOPMENTAL DISORDER WITH POOR GROWTH AND WITH OR WITHOUT SEIZURES OR ATAXIA  
Intellectual Developmental Disorder with Seizures and Language Delay  
intellectual disability and myopathy syndrome  
Joubert syndrome 10  
Joubert syndrome 3  
Joubert syndrome 5  
Ketoadipicaciduria 
Kifafa Seizure Disorder 
Kilquist Syndrome  
KINSSHIP syndrome  
Kohlschutter-Tonz syndrome  
Koolen de Vries syndrome  
Luo-Schoch-Yamamoto syndrome  
Maxillofacial Dysostosis 
MEHMO syndrome  
Mental Retardation, Microcephaly, Epilepsy, and Coarse Face 
Microcephaly, Epilepsy, and Diabetes Syndrome +   
microcephaly, growth deficiency, seizures, and brain malformations  
Midface Hypoplasia, Obesity, Developmental Delay, and Neonatal Hypotonia 
multiple congenital anomalies-hypotonia-seizures syndrome +   
mutism  
Myoclonic Epilepsies +   
Myopathy, Epilepsy, and Progressive Cerebral Atrophy  
neonatal lethal pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome  
NESCAV syndrome  
NEURODEGENERATION AND SEIZURES DUE TO COPPER TRANSPORT DEFECT  
NEURODEGENERATION WITH DEVELOPMENTAL DELAY, EARLY RESPIRATORY FAILURE, MYOCLONIC SEIZURES, AND BRAIN ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER AND STRUCTURAL BRAIN ANOMALIES WITH OR WITHOUT SEIZURES AND SPASTICITY  
NEURODEVELOPMENTAL DISORDER WITH ABSENT LANGUAGE AND VARIABLE SEIZURES  
NEURODEVELOPMENTAL DISORDER WITH ABSENT SPEECH AND MOVEMENT AND BEHAVIORAL ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH ATAXIA, HYPOTONIA, AND MICROCEPHALY  
NEURODEVELOPMENTAL DISORDER WITH BEHAVIORAL ABNORMALITIES, ABSENT SPEECH, AND HYPOTONIA  
NEURODEVELOPMENTAL DISORDER WITH CENTRAL HYPOTONIA AND DYSMORPHIC FACIES  
NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES  
neurodevelopmental disorder with dysmorphic facies and behavioral abnormalities  
neurodevelopmental disorder with dysmorphic facies and distal limb anomalies  
neurodevelopmental disorder with dysmorphic facies and thin corpus callosum  
Neurodevelopmental Disorder with Dysmorphic Facies and Variable Seizures  
NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, IMPAIRED SPEECH, AND HYPOTONIA  
NEURODEVELOPMENTAL DISORDER WITH DYSTONIA AND SEIZURES  
NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND BRAIN ATROPHY  
NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HEMOCHROMATOSIS  
NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HYPOPLASIA OF THE CORPUS CALLOSUM  
Neurodevelopmental Disorder with Epilepsy, Cataracts, Feeding Difficulties, and Delayed Brain Myelination  
Neurodevelopmental Disorder with Epilepsy, Spasticity, and Brain Atrophy  
neurodevelopmental disorder with eye movement abnormalities and ataxia  
neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities  
NEURODEVELOPMENTAL DISORDER WITH HYPERKINETIC MOVEMENTS, SEIZURES, AND STRUCTURAL BRAIN ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND AUTISTIC FEATURES WITH OR WITHOUT HYPERKINETIC MOVEMENTS  
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND BRAIN ABNORMALITIES  
Neurodevelopmental Disorder with Hypotonia and Cerebellar Atrophy, with or without Seizures  
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND DYSMORPHIC FACIES  
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND GROSS MOTOR AND SPEECH DELAY  
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND SEIZURES  
neurodevelopmental disorder with hypotonia and speech delay  
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, BRAIN ANOMALIES, DISTINCTIVE FACIES, AND ABSENT LANGUAGE  
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, DYSMORPHIC FACIES, AND SKELETAL ANOMALIES, WITH OR WITHOUT SEIZURES  
Neurodevelopmental Disorder with Hypotonia, Dysmorphic Facies, and Skin Abnormalities  
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, FACIAL DYSMORPHISM, AND BRAIN ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, FEEDING DIFFICULTIES, FACIAL DYSMORPHISM, AND BRAIN ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, IMPAIRED SPEECH, AND BEHAVIORAL ABNORMALITIES  
neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures  
Neurodevelopmental Disorder with Hypotonia, Microcephaly, and Seizures   
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEONATAL RESPIRATORY INSUFFICIENCY, AND THERMODYSREGULATION  
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE  
neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language  
An autosomal dominant intellectual developmental disorder that is characterized by global developmental delay with hypotonia, poor motor development with limited walking, impaired intellectual development with poor or absent speech, and behavioral abnormalities and that has_material_basis_in an autosomal dominant mutation of the MEF2C gene on chromosome 5q14.3. (DO)
Neurodevelopmental Disorder with Impaired Intellectual Development, Hypotonia, and Ataxia   
NEURODEVELOPMENTAL DISORDER WITH IMPAIRED LANGUAGE AND ATAXIA AND WITH OR WITHOUT SEIZURES  
Neurodevelopmental Disorder with Impaired Speech and Hyperkinetic Movements  
NEURODEVELOPMENTAL DISORDER WITH INFANTILE EPILEPTIC SPASMS  
NEURODEVELOPMENTAL DISORDER WITH LANGUAGE DELAY AND BEHAVIORAL ABNORMALITIES, WITH OR WITHOUT SEIZURES  
neurodevelopmental disorder with language delay and seizures  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND SPEECH DELAY, WITH OR WITHOUT BRAIN ABNORMALITIES  
neurodevelopmental disorder with microcephaly, absent speech, and hypotonia  
Neurodevelopmental Disorder with Microcephaly, Epilepsy, and Hypomyelination  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND ABSENT LANGUAGE  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, NYSTAGMUS, AND SEIZURES  
Neurodevelopmental Disorder with Microcephaly, Impaired Language, Epilepsy, and Gait Abnormalities  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, MOVEMENT ABNORMALITIES, AND SEIZURES  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND BRAIN ATROPHY  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND NEONATAL CHOLESTASIS  
NEURODEVELOPMENTAL DISORDER WITH MOTOR ABNORMALITIES, SEIZURES, AND FACIAL DYSMORPHISM  
NEURODEVELOPMENTAL DISORDER WITH NONSPECIFIC BRAIN ABNORMALITIES AND WITH OR WITHOUT SEIZURES  
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT EARLY-ONSET GENERALIZED EPILEPSY  
neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures  
Neurodevelopmental Disorder with Seizures and Brain Abnormalities  
NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND BRAIN ATROPHY  
NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND GINGIVAL OVERGROWTH  
Neurodevelopmental Disorder with Seizures and Nonepileptic Hyperkinetic Movements  
Neurodevelopmental Disorder with Seizures and Speech and Walking Impairment  
NEURODEVELOPMENTAL DISORDER WITH SEIZURES, HYPOTONIA, AND BRAIN IMAGING ABNORMALITIES  
Neurodevelopmental Disorder with Seizures, Microcephaly, and Brain Abnormalities  
NEURODEVELOPMENTAL DISORDER WITH SEIZURES, SPASTICITY, AND COMPLETE OR PARTIAL AGENESIS OF THE CORPUS CALLOSUM  
NEURODEVELOPMENTAL DISORDER WITH SPASTICITY, SEIZURES, AND BRAIN ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH SPEECH DELAY AND VARIABLE OCULAR ANOMALIES  
neurodevelopmental disorder with speech impairment and dysmorphic facies  
NEUROMUSCULAR DISORDER, CONGENITAL, WITH DYSMORPHIC FACIES  
Neuronal Ceroid Lipofuscinosis 15  
NEUROOCULAR SYNDROME 2, PAROXYSMAL TYPE  
Non-Lissencephalic Cortical Dysplasia 
Okur-Chung Neurodevelopmental Syndrome  
ONYCHODYSTROPHY, OSTEODYSTROPHY, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES SYNDROME  
Opticocochleodentate Degeneration 
osteosclerotic metaphyseal dysplasia  
pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures  
PEHO-like syndrome  
Photogenic Epilepsy with Spastic Diplegia and Mental Retardation 
Pierpont syndrome  
Pitt-Hopkins syndrome +   
POIRIER-BIENVENU NEURODEVELOPMENTAL SYNDROME  
polyhydramnios, megalencephaly, and symptomatic epilepsy  
Popov-Chang Syndrome 
Post-Traumatic Epilepsy 
Progressive Encephalopathy with Amyotrophy and Optic Atrophy  
Progressive Microcephaly with Seizures and Cerebral and Cerebellar Atrophy  
Psychomotor Retardation, Epilepsy, and Craniofacial Dysmorphism  
pyridoxamine 5'-phosphate oxidase deficiency  
pyridoxine-dependent epilepsy +   
Qazi Markouizos syndrome 
RADIO-TARTAGLIA SYNDROME  
Ramon Syndrome 
Retinal Degeneration and Epilepsy 
ROLANDIC EPILEPSY, INTELLECTUAL DISABILITY, AND SPEECH DYSPRAXIA, X-LINKED  
Rud Syndrome 
salt and pepper syndrome  
Sandhaus Ben-Ami Syndrome 
scalp-ear-nipple syndrome  
Schuurs-Hoeijmakers syndrome  
Seizures, Cortical Blindness, and Microcephaly Syndrome  
SEIZURES, EARLY-ONSET, WITH NEURODEGENERATION AND BRAIN CALCIFICATIONS  
SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME  
SHORT STATURE, IMPAIRED INTELLECTUAL DEVELOPMENT, MICROCEPHALY, HYPOTONIA, AND OCULAR ANOMALIES  
Sifrim-Hitz-Weiss syndrome  
Snijders Blok-Fisher Syndrome  
SPASTIC TETRAPLEGIA AND AXIAL HYPOTONIA, PROGRESSIVE  
Speech Disturbance - Use of Faulty Phrasing and Unrelated Words 
speech-language disorder-1  
Spinocerebellar Ataxia with Epilepsy  
status epilepticus +   
Stomatin-Deficient Cryohydrocytosis with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly  
stress-induced childhood-onset neurodegeneration with variable ataxia and seizures  
syndromic X-linked intellectual disability Hedera type  
Tessadori-Bicknell-van Haaften neurodevelopmental syndrome 1  
Unilateral Radioulnar Synostosis with Developmental Retardation and Hypotonia 
USMANI-RIAZUDDIN SYNDROME, AUTOSOMAL DOMINANT  
Vissers-Bodmer syndrome  
visual epilepsy +   
Vulto-van Silfout-de Vries syndrome  
Webb-Dattani Syndrome  
WHITE-KERNOHAN SYNDROME  
White-Sutton syndrome  
Wittwer Syndrome  
X-linked Epilepsy 2 with or without Impaired Intellectual Development and Dysmorphic Features  
X-linked epilepsy with variable learning disabilities and behavior disorders  
Xia-Gibbs syndrome  

Synonyms
Exact Synonyms: INTELLECTUAL DISABILITY, STEREOTYPIC MOVEMENTS, EPILEPSY, AND/OR CEREBRAL MALFORMATIONS ;   MEF2C-RELATED CONDITION ;   MEF2C-RELATED DISORDER ;   MRD20 ;   Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations ;   autosomal dominant mental retardation 20
Narrow Synonyms: CHROMOSOME 5q14.3 DELETION SYNDROME, PROXIMAL
Primary IDs: MIM:613443
Definition Sources: PMID:20513142 "DO" "DO"

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