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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
ALKURAYA-KUCINSKAS SYNDROME  
Attention Deficit and Disruptive Behavior Disorders +   
BAKER-GORDON SYNDROME  
Cerebellar Hypoplasia with Endosteal Sclerosis  
Child Behavior Disorders +   
Childhood Schizophrenia  
communication disorder +   
developmental coordination disorder  
Developmental Delay with Variable Intellectual Impairment and Behavioral Abnormalities  
Developmental Disabilities +   
Disorders in which there is a delay in development based on that expected for a given age level or stage of development. These impairments or disabilities originate before age 18, may be expected to continue indefinitely, and constitute a substantial impairment. Biological and nonbiological factors are involved in these disorders. (From American Psychiatric Glossary, 6th ed)
Diencephalic-Mesencephalic Junction Dysplasia Syndromes +   
GABRIELE-DE VRIES SYNDROME  
HAREL-YOON SYNDROME  
IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES  
INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE AND VARIABLE SKELETAL ANOMALIES  
intellectual disability +   
JABERI-ELAHI SYNDROME  
Kahn-Kahn-Katsanis Syndrome  
learning disability +   
Lopes-Maciel-Rodan Syndrome  
Mitochondrial Neurodevelopmental Disorder, with Abnormal Movements and Lactic Acidosis, with or without Seizures  
mutism  
Neurodevelopmental Disorder and Language Delay with or Without Structural Brain Abnormalities  
NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER  
NEURODEVELOPMENTAL DISORDER WITH CATARACTS, POOR GROWTH, AND DYSMORPHIC FACIES  
Neurodevelopmental Disorder with Central and Peripheral Motor Dysfunction  
NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES  
NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR HYPOPLASIA AND SPASTICITY  
NEURODEVELOPMENTAL DISORDER WITH COARSE FACIES AND MILD DISTAL SKELETAL ABNORMALITIES;   
NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES  
NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HYPOPLASIA OF THE CORPUS CALLOSUM  
NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION  
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE  
Neurodevelopmental Disorder with Impaired Intellectual Development, Hypotonia, and Ataxia   
Neurodevelopmental Disorder with Impaired Speech and Hyperkinetic Movements  
NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENTS  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND STRUCTURAL BRAIN ANOMALIES  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ARTHROGRYPOSIS, AND STRUCTURAL BRAIN ANOMALIES  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ATAXIA, AND SEIZURES  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND BRAIN ATROPHY  
Neurodevelopmental Disorder with Microcephaly, Epilepsy, and Hypomyelination  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY  
NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES  
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART  
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE  
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT VARIABLE BRAIN ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES  
NEURODEVELOPMENTAL DISORDER WITH REGRESSION, ABNORMAL MOVEMENTS, LOSS OF SPEECH, AND SEIZURES  
NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND NONEPILEPTIC HYPERKINETIC MOVEMENTS  
NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND SPEECH AND WALKING IMPAIRMENT  
NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE  
NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA AND BRAIN ABNORMALITIES WITH OR WITHOUT SEIZURES  
NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH  
Neurodevelopmental Disorder with Structural Brain Anomalies and Dysmorphic Facies  
NEURODEVELOPMENTAL DISORDER WITH VISUAL DEFECTS AND BRAIN ANOMALIES  
O'DONNELL-LURIA-RODAN SYNDROME  
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME  
Pervasive Child Development Disorders +   
PILAROWSKI-BJORNSSON SYNDROME  
Popov-Chang Syndrome  
Reactive Attachment Disorder 
separation anxiety disorder  
SHUKLA-VERNON SYNDROME  
Skraban-Deardorff Syndrome  
Spastic Paraplegia and Psychomotor Retardation with or without Seizures  
STANKIEWICZ-ISIDOR SYNDROME  
stereotypic movement disorder +   
tic disorder +   
Trichohepatoneurodevelopmental Syndrome  
Ventriculomegaly  
X-Linked Neurodevelopmental Disorder with Craniofacial Abnormalities  
 3MC syndrome 3  
 Abuse Dwarfism Syndrome 
 AGAT deficiency  
 Al Gazali Sabrinathan Nair Syndrome 
 Arthrogryposis, Cleft Palate, Craniosynostosis, and Impaired Intellectual Development  
 Bagatelle Cassidy syndrome 
 Bainbridge-Ropers Syndrome  
 Beaulieu-Boycott-Innes Syndrome  
 Bosch-Boonstra-Schaaf Optic Atrophy Syndrome  
 Brachycephaly, Trichomegaly, and Developmental Delay  
 CEREBELLAR ATROPHY WITH SEIZURES AND VARIABLE DEVELOPMENTAL DELAY  
 CEREBELLAR ATROPHY, DEVELOPMENTAL DELAY, AND SEIZURES  
 Cerebellar Hypoplasia +   
 Cerebellofaciodental Syndrome  
 Chitayat Moore Del Bigio Syndrome 
 Chitty Hall Webb Syndrome 
 Chondrodysplasia, Megarbane-Dagher-Melki Type  
 chromosome 13q14 deletion syndrome  
 chromosome 17p13.3 duplication syndrome  
 chromosome 3q29 microdeletion syndrome 
 chromosome Xp11.23-p11.22 duplication syndrome 
 Cohen Syndrome  
 CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY  
 CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER  
 CONGENITAL HYPOTONIA, EPILEPSY, DEVELOPMENTAL DELAY, AND DIGITAL ANOMALIES  
 Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation 
 Der Kaloustian Mcintosh Silver Syndrome 
 Desanto-Shinawi Syndrome  
 DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM  
 DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES  
 Diencephalic-Mesencephalic Junction Dysplasia Syndrome 2  
 Dyskinesias, Seizures, and Intellectual Developmental Disorder  
 Forebrain Defects  
 Forsythe-Wakeling Syndrome 
 Fragile Site 16p12 
 GLOBAL DEVELOPMENTAL DELAY WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT  
 GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES  
 Global Developmental Delay, Lung Cysts, Overgrowth, and Wilms Tumor  
 Global Developmental Delay, Progressive Ataxia, and Elevated Glutamine  
 Growth Retardation, Developmental Delay, Coarse Facies, and Early Death  
 Grubben de Cock Borghgraef Syndrome 
 Heyn-Sproul-Jackson Syndrome 
 hypermethioninemia due to adenosine kinase deficiency  
 HYPOPIGMENTATION, ORGANOMEGALY, AND DELAYED MYELINATION AND DEVELOPMENT  
 HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME  
 HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME  
 IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA  
 Kat6a Syndrome  
 Keppen-Lubinsky Syndrome  
 Lamb-Shaffer Syndrome  
 Loucks-Innes Syndrome  
 Luscan-Lumish syndrome  
 Microcephaly, Cataracts, Impaired Intellectual Development, and Dystonia with Abnormal Striatum  
 Microcephaly, Growth Retardation, Cataract, Hearing Loss, and Unusual Appearance 
 microcephaly, seizures, and developmental delay  
 Midface Hypoplasia, Obesity, Developmental Delay, and Neonatal Hypotonia 
 Mitochondrial Progressive Myopathy with Congenital Cataract, Hearing Loss, and Developmental Delay  
 Non-Lissencephalic Cortical Dysplasia 
 Obesity, Hyperphagia, and Developmental Delay  
 Ogden syndrome  
 Oliver-McFarlane syndrome  
 Osteosclerotic Metaphyseal Dysplasia  
 Partington Anderson Syndrome 
 Periventricular Nodular Heterotopia with Syndactyly, Cleft Palate and Developmental Delay  
 Pierpont syndrome  
 Pseudo-TORCH Syndrome +   
 Rajab Syndrome  
 Refsum Disease with Increased Pipecolic Acidemia 
 Rhizomelic Short Stature with Microcephaly, Micrognathia, and Developmental Delay  
 Roifman-Chitayat Syndrome 
 Short Stature, Developmental Delay, and Congenital Heart Defects  
 SIDDIQI SYNDROME  
 sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay  
 SNIJDERS BLOK-FISHER SYNDROME  
 Stiff Thumbs, with Brachydactyly Type A1 and Developmental Delay 
 succinic semialdehyde dehydrogenase deficiency  
 Ter Haar Syndrome  
 Tetra Amelia with Ectodermal Dysplasia and Lacrimal Duct Abnormalities 
 Turnpenny-Fry Syndrome  
 Unilateral Radioulnar Synostosis with Developmental Retardation and Hypotonia 
 VERVERI-BRADY SYNDROME  
 WEISS-KRUSZKA SYNDROME  

Synonyms
Exact Synonyms: Child Development Deviation ;   Child Development Deviations ;   Child Development Disorder ;   Child Development Disorders ;   Child Development Disorders, Specific ;   DEVELOPMENTAL DELAY ;   Developmental Delay Disorder ;   Developmental Delay Disorders ;   Developmental Disability ;   Global developmental delay
Primary IDs: MESH:D002658 ;   RDO:0000673
Definition Sources: MESH:D002658

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