Attention Deficit-Hyperactivity Disorder |
|
Hyperactivity, Attention deficit hyperactivity disorder |
OMIM:143465 |
Intellectual Developmental Disorder, Autosomal Recessive 54 |
|
Hyperactivity |
OMIM:617028 |
Cephalin Lipidosis |
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Abnormality of the spleen |
OMIM:212800 |
Schizophrenia 15 |
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Hyperactivity |
OMIM:613950 |
Immunodeficiency 8 |
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Hyperactivity, Lymphopenia |
OMIM:615401 |
Mental Retardation, Autosomal Dominant 45 |
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Hyperactivity, Attention deficit hyperactivity disorder |
OMIM:617600 |
22q13 deletion syndrome (Phelan-Mcdermid syndrome) |
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Hyperactivity |
DECIPHER:20 |
Mental Retardation, Autosomal Recessive 2 |
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Attention deficit hyperactivity disorder |
OMIM:607417 |
Potocki-Lupski syndrome (17p11.2 duplication syndrome) |
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Hyperactivity |
DECIPHER:19 |
Mental Retardation, Autosomal Recessive 3 |
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Hyperactivity |
OMIM:608443 |
Autism, Susceptibility To, 20 |
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Attention deficit hyperactivity disorder |
OMIM:618830 |
Intellectual Disability-Expressive Aphasia-Facial Dysmorphism Syndrome |
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Hyperactivity, Cafe-au-lait spot |
ORPHA:436151 |
Developmental And Epileptic Encephalopathy 43 |
|
Hyperactivity, Ataxia |
OMIM:617113 |
Mental Retardation, Autosomal Dominant 52 |
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Hyperactivity |
OMIM:617796 |
Mental Retardation, Autosomal Dominant 33 |
|
Hyperactivity |
OMIM:616311 |
Spastic Tetraplegia, Thin Corpus Callosum, And Progressive Microcephaly |
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Hyperactivity, Inability to walk |
OMIM:616657 |
Mental Retardation, Autosomal Recessive 37 |
|
Hyperactivity |
OMIM:615493 |
Ank3-Related Intellectual Disability-Sleep Disturbance Syndrome |
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Hyperactivity |
ORPHA:356996 |
Hyperpigmentation With Or Without Hypopigmentation, Familial Progressive |
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Hypopigmented skin patches, Vitiligo, Multiple lentigines, Progressive hyperpigmentation, Hyperme... |
OMIM:145250 |
Intellectual Developmental Disorder, X-Linked 72 |
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Hyperactivity |
OMIM:300271 |
Intellectual Developmental Disorder, Autosomal Recessive 74 |
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Hyperactivity |
OMIM:617169 |
Mental Retardation, X-Linked 77 |
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Hyperactivity |
OMIM:300454 |
Language Delay And Attention Deficit-Hyperactivity Disorder/Cognitive Impairment With Or Without Cardiac Arrhythmia |
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Hyperactivity, Attention deficit hyperactivity disorder |
OMIM:617182 |
Microcephaly, Seizures, And Developmental Delay |
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Hyperactivity, Ataxia |
OMIM:613402 |
Smith-Magenis syndrome |
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Hyperactivity |
DECIPHER:8 |
Neurodevelopmental Disorder With Epilepsy And Hypoplasia Of The Corpus Callosum |
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Dysmetria, Gait disturbance, Inability to walk, Hyperactivity |
OMIM:618090 |
Insulin-Like Growth Factor I Deficiency |
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Hyperactivity |
OMIM:608747 |
Encephalopathy, Progressive, With Or Without Lipodystrophy |
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Dystonia, Hepatomegaly, Hyperactivity, Ataxia |
OMIM:615924 |
Intellectual Developmental Disorder, X-Linked, Syndromic, Houge Type |
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Hyperactivity, Attention deficit hyperactivity disorder |
OMIM:301008 |
Aminoacylase 1 Deficiency |
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Hyperactivity |
OMIM:609924 |
Juvenile Huntington Disease |
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Dystonia, Bradykinesia, Hyperactivity, Progressive cerebellar ataxia, Ataxia, Broad-based gait, G... |
ORPHA:248111 |
Intellectual Developmental Disorder, X-Linked 101 |
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Hyperactivity |
OMIM:300928 |
X-Linked Intellectual Disability, Stocco Dos Santos Type |
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Hyperactivity |
ORPHA:85288 |
Hyperprolinemia, Type I |
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Hyperactivity, Ataxia |
OMIM:239500 |
Intellectual Developmental Disorder With Epilepsy, Behavioral Abnormalities, And Coarse Facies |
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Hyperactivity |
OMIM:619031 |
Microcephaly 2, Primary, Autosomal Recessive, With Or Without Cortical Malformations |
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Hyperactivity |
OMIM:604317 |
Hyperlysinemia, Type I |
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Hyperactivity, Anemia |
OMIM:238700 |
Glycine Encephalopathy |
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Hyperactivity, Lethargy |
OMIM:605899 |
8p23.1 deletion syndrome |
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Hyperactivity |
DECIPHER:39 |
Angelman Syndrome Due To Imprinting Defect In 15Q11-Q13 |
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Hyperactivity, Ataxia, Broad-based gait, Hypopigmentation of the skin |
ORPHA:411515 |
Mannosidosis, Beta A, Lysosomal |
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Hyperactivity |
OMIM:248510 |
Morm Syndrome |
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Hyperactivity |
ORPHA:75858 |
X-Linked Intellectual Disability-Hypotonia-Movement Disorder Syndrome |
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Abnormality of skin pigmentation, Hyperactivity, Broad-based gait |
ORPHA:457260 |
Phenylketonuria |
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Hyperactivity, Attention deficit hyperactivity disorder, Generalized hypopigmentation |
OMIM:261600 |
Dihydropyrimidine Dehydrogenase Deficiency |
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Hyperactivity, Lethargy |
OMIM:274270 |
Intellectual Developmental Disorder, X-Linked 104 |
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Hyperactivity, Ataxia |
OMIM:300983 |
Intellectual Developmental Disorder, X-Linked 109 |
|
Hyperactivity |
OMIM:309548 |
Fraxe Intellectual Disability |
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Hyperactivity |
ORPHA:100973 |
Neurodevelopmental Disorder With Motor And Speech Delay And Behavioral Abnormalities |
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Hyperactivity, Broad-based gait |
OMIM:619470 |
Intellectual Developmental Disorder, X-Linked, Syndromic, Stocco Dos Santos Type |
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Hyperactivity |
OMIM:300434 |
Intellectual Developmental Disorder, Autosomal Recessive 39 |
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Hyperactivity |
OMIM:615541 |
Mental Retardation, Autosomal Dominant 43 |
|
Hyperactivity |
OMIM:616977 |
Chromosome 3Q29 Deletion Syndrome |
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Hyperactivity, Gait ataxia |
OMIM:609425 |
Coffin-Siris Syndrome 8 |
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Hyperactivity |
OMIM:618362 |
Xq25 Microduplication Syndrome |
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Hyperactivity |
ORPHA:521258 |
Chromosome Xq25 Duplication Syndrome |
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Hyperactivity |
OMIM:300979 |
Dystonia, Dopa-Responsive, Due To Sepiapterin Reductase Deficiency |
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Hyperactivity, Dystonia, Ataxia |
OMIM:612716 |
Lennox-Gastaut Syndrome |
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Hyperactivity, Falls |
ORPHA:2382 |
Optic Atrophy 11 |
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Dysmetria, Hyperactivity, Ataxia |
OMIM:617302 |
Severe Neurodegenerative Syndrome With Lipodystrophy |
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Hepatomegaly, Cirrhosis, Hepatic steatosis, Hyperactivity, Ataxia, Gait ataxia, Limb dystonia |
ORPHA:363400 |
Gand Syndrome |
|
Hyperactivity |
OMIM:615074 |
Guanidinoacetate Methyltransferase Deficiency |
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Hyperactivity, Dystonia, Athetosis, Ataxia |
ORPHA:382 |
Neurodevelopmental Disorder With Movement Abnormalities, Abnormal Gait, And Autistic Features |
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Unsteady gait, Hyperactivity, Broad-based gait |
OMIM:617865 |
Chromosome 15Q25 Deletion Syndrome |
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Hyperactivity, Macrocytic anemia, Attention deficit hyperactivity disorder |
OMIM:614294 |
Landau-Kleffner Syndrome |
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Steppage gait, Hyperactivity, Attention deficit hyperactivity disorder, Gait ataxia |
ORPHA:98818 |
Cln5 Disease |
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Dysmetria, Hyperactivity, Inability to walk, Dysdiadochokinesis, Ataxia, Truncal ataxia, Unsteady... |
ORPHA:228360 |
Intellectual Developmental Disorder, Autosomal Recessive 71 |
|
Hyperactivity, Attention deficit hyperactivity disorder |
OMIM:618504 |
Mucopolysaccharidosis, Type Iiia |
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Hyperactivity, Hepatomegaly, Splenomegaly |
OMIM:252900 |
Neurodevelopmental Disorder With Behavioral Abnormalities, Absent Speech, And Hypotonia |
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Hyperactivity, Inability to walk |
OMIM:618718 |
Mental Retardation, Autosomal Recessive 13 |
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Hyperactivity |
OMIM:613192 |
Intellectual Developmental Disorder, Autosomal Recessive 38 |
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Unsteady gait, Hyperactivity |
OMIM:615516 |
Childhood-Onset Motor And Cognitive Regression Syndrome With Extrapyramidal Movement Disorder |
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Hyperactivity, Dystonia, Inability to walk, Gait ataxia |
ORPHA:500180 |
X-Linked Intellectual Disability-Psychosis-Macroorchidism Syndrome |
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Hyperactivity, Shuffling gait, Broad-based gait |
ORPHA:3077 |
Intellectual Developmental Disorder, X-Linked 107 |
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Hyperactivity, Attention deficit hyperactivity disorder |
OMIM:301013 |
Succinic Semialdehyde Dehydrogenase Deficiency |
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Hyperactivity, Ataxia |
OMIM:271980 |
Myopathy With Extrapyramidal Signs |
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Dystonia, Leukocytosis, Hepatomegaly, Splenomegaly, Hyperactivity, Ataxia, Difficulty walking |
OMIM:615673 |
Rasmussen Subacute Encephalitis |
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Hyperactivity, Hemidystonia, Attention deficit hyperactivity disorder, Inability to walk |
ORPHA:1929 |
Mucopolysaccharidosis, Type Iiib |
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Hyperactivity, Hepatomegaly, Splenomegaly |
OMIM:252920 |
Purine Nucleoside Phosphorylase Deficiency |
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Abnormal T cell morphology, Decreased proportion of CD3-positive T cells, Hyperactivity, Autoimmu... |
ORPHA:760 |
Legius Syndrome |
|
Dystonia, Acute monocytic leukemia, Hyperactivity, Inguinal freckling, Axillary freckling, Multip... |
ORPHA:137605 |
Mitochondrial Complex Iii Deficiency, Nuclear Type 7 |
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Hyperactivity |
OMIM:615824 |
Intellectual Developmental Disorder, X-Linked, Syndromic, Snijders Blok Type |
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Hyperactivity, Broad-based gait |
OMIM:300958 |
Growth Delay Due To Insulin-Like Growth Factor Type 1 Deficiency |
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Hyperactivity, Attention deficit hyperactivity disorder, Cafe-au-lait spot |
ORPHA:73272 |
Fragile X Syndrome |
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Hyperactivity |
OMIM:300624 |
Intellectual Developmental Disorder, X-Linked 21 |
|
Hyperactivity |
OMIM:300143 |
Graves Disease, Susceptibility To, 1 |
|
Hyperactivity |
OMIM:275000 |
Myoclonic-Astatic Epilepsy |
|
Unsteady gait, Hyperactivity, Attention deficit hyperactivity disorder, Ataxia |
ORPHA:1942 |
Macrocephaly-Intellectual Disability-Neurodevelopmental Disorder-Small Thorax Syndrome |
|
Hypopigmented skin patches, Gait disturbance, Hyperactivity, Cafe-au-lait spot |
ORPHA:457485 |
Histidinemia |
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Hyperactivity |
ORPHA:2157 |
Angelman Syndrome Due To Maternal 15Q11Q13 Deletion |
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Gait imbalance, Hypopigmentation of the skin, Ataxia, Hyperactivity, Broad-based gait |
ORPHA:98794 |
Mucopolysaccharidosis, Type Iiic |
|
Hyperactivity, Hepatomegaly, Splenomegaly |
OMIM:252930 |
X-Linked Creatine Transporter Deficiency |
|
Hyperactivity, Dystonia, Athetosis, Ataxia |
ORPHA:52503 |
Female Restricted Epilepsy With Intellectual Disability |
|
Hyperactivity |
ORPHA:101039 |
Infantile Neuroaxonal Dystrophy |
|
Dystonia, Gait disturbance, Hyperactivity, Ataxia, Unsteady gait |
ORPHA:35069 |
Angelman Syndrome |
|
Hyperactivity, Broad-based gait, Progressive gait ataxia, Hypopigmentation of the skin |
OMIM:105830 |
Neurodevelopmental Disorder With Coarse Facies And Mild Distal Skeletal Abnormalities |
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Hyperactivity, Hypermelanotic macule, Cafe-au-lait spot |
OMIM:618505 |
Bone Marrow Failure Syndrome 3 |
|
Abnormality of skin pigmentation, Bone marrow hypocellularity, Acute myeloid leukemia, Hyperactiv... |
OMIM:617052 |
Mucopolysaccharidosis, Type Iiid |
|
Hyperactivity, Hepatomegaly, Splenomegaly |
OMIM:252940 |
Severe Intellectual Disability-Short Stature-Behavioral Abnormalities-Facial Dysmorphism Syndrome |
|
Hyperactivity, Lymphopenia |
ORPHA:391307 |
X-Linked Intellectual Disability-Acromegaly-Hyperactivity Syndrome |
|
Hyperactivity |
ORPHA:85327 |
Hypomagnesemia, Seizures, And Mental Retardation 2 |
|
Hyperactivity |
OMIM:618314 |
Neurodevelopmental Disorder With Or Without Autism Or Seizures |
|
Hyperactivity |
OMIM:619239 |
Neurodegeneration With Brain Iron Accumulation 1 |
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Gait disturbance, Dystonia, Acanthocytosis, Hyperpigmentation of the skin, Bradykinesia, Hyperact... |
OMIM:234200 |
Pediatric-Onset Graves Disease |
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Hepatomegaly, Neutropenia in presence of anti-neutropil antibodies, Splenomegaly, Hyperactivity, ... |
ORPHA:525731 |
Argininemia |
|
Hepatomegaly, Portal fibrosis, Spastic gait, Micronodular cirrhosis, Hyperactivity, Cholestasis |
OMIM:207800 |
Neurodegeneration With Brain Iron Accumulation 2B |
|
Dystonia, Dysmetria, Bradykinesia, Hyperactivity, Dysdiadochokinesis, Gait ataxia |
OMIM:610217 |
X-Linked Adrenoleukodystrophy |
|
Hyperactivity, Gait disturbance, Attention deficit hyperactivity disorder |
ORPHA:43 |
Citrullinemia Type Ii |
|
Hepatomegaly, Hepatic fibrosis, Hepatocellular carcinoma, Pancreatitis, Hepatic steatosis, Hypera... |
ORPHA:247585 |
Pitt-Hopkins-Like Syndrome 1 |
|
Hyperactivity, Ataxia |
OMIM:610042 |
Nijmegen Breakage Syndrome |
|
B lymphocytopenia, Progressive vitiligo, Hyperactivity, Autoimmune hemolytic anemia, Thrombocytop... |
OMIM:251260 |
X-Linked Cerebral Adrenoleukodystrophy |
|
Gait disturbance, Dysmetria, Hyperactivity, Inability to walk, Ataxia, Difficulty walking |
ORPHA:139396 |
Hyperthyroidism, Nonautoimmune |
|
Hyperactivity |
OMIM:609152 |
Spastic Paraplegia 29, Autosomal Dominant |
|
Hyperactivity |
OMIM:609727 |
47,Xyy Syndrome |
|
Hyperactivity, Attention deficit hyperactivity disorder |
ORPHA:8 |
Noonan Syndrome-Like Disorder With Loose Anagen Hair 1 |
|
Hyperpigmentation of the skin, Hyperactivity, Multiple lentigines, Attention deficit hyperactivit... |
OMIM:607721 |
Neurodevelopmental Disorder With Impaired Speech And Hyperkinetic Movements |
|
Torticollis, Dystonia, Ataxia |
OMIM:618425 |
Oculoectodermal Syndrome |
|
Hyperactivity, Hyperpigmentation of the skin |
OMIM:600268 |
Familial Gestational Hyperthyroidism |
|
Hyperactivity |
ORPHA:99819 |
Familial Hyperthyroidism Due To Mutations In Tsh Receptor |
|
Hyperactivity |
ORPHA:424 |
Cerebellar Dysfunction With Variable Cognitive And Behavioral Abnormalities |
|
Dysmetria, Hyperactivity, Unsteady gait, Ataxia |
OMIM:614756 |
Choreoacanthocytosis |
|
Hepatomegaly, Lingual dystonia, Acanthocytosis, Loss of ambulation, Oromandibular dystonia, Falls... |
ORPHA:2388 |
Tuberous Sclerosis Complex |
|
Hypomelanotic macule, Hepatic cysts, Pulmonary lymphangiomyomatosis, Hyperactivity, Attention def... |
ORPHA:805 |