Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandMental Disorders Diagnosed in Childhood (D019952)
..Starting node
..expandDevelopmental Disabilities (D002658)

       Child Nodes:
........expandAbuse dwarfism syndrome (C535569)
........expandAl Gazali Sabrinathan Nair syndrome (C535617)
........expandArginine:Glycine Amidinotransferase Deficiency (C567192)
........expandBagatelle Cassidy syndrome (C537796)
........expandBAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA (OMIM:251290)
........expandBEAULIEU-BOYCOTT-INNES SYNDROME (OMIM:613680)
........expandCerebellar Hypoplasia (C562568)
........expandChitayat Moore Del Bigio syndrome (C535927)
........expandChitty Hall Webb syndrome (C535929)
........expandChondrodysplasia, Megarbane-Dagher-Melki Type (C567644)
........expandCHROMOSOME 13q14 DELETION SYNDROME (OMIM:613884)
........expandChromosome 17p13.3 Duplication Syndrome (C567705)
........expandChromosome 3q29 Deletion Syndrome (C567184)
........expandChromosome Xp11.23-P11.22 Duplication Syndrome (C567585)
........expandCohen syndrome (C536438)
........expandCraniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation (C564271)
........expandDer Kaloustian Mcintosh Silver syndrome (C538217)
........expandForebrain Defects (C566067)
........expandFORSYTHE-WAKELING SYNDROME (OMIM:613606)
........expandFragile Site 16p12 (C565001)
........expandGrowth Retardation, Developmental Delay, Coarse Facies, And Early Death (C567856)
........expandGrubben de Cock Borghgraef syndrome (C537621)
........expandMalpuech facial clefting syndrome (C535704)
........expandMicrocephaly, Growth Retardation, Cataract, Hearing Loss, And Unusual Appearance (C567849)
........expandMICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY (OMIM:613402)
........expandMidface Hypoplasia, Obesity, Developmental Delay, and Neonatal Hypotonia (C563896)
........expandMyopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay (C567769)
........expandNon-lissencephalic cortical dysplasia (C536243)
........expandObesity, Hyperphagia, and Developmental Delay (C563938)
........expandOliver-McFarlane syndrome (C536554)
........expandPartington Anderson syndrome (C536299)
........expandPlantar Lipomatosis, Unusual Facies, and Developmental Delay (C566559)
........expandRadioulnar Synostosis, Unilateral, with Developmental Retardation and Hypotonia (C564856)
........expandRAJAB SYNDROME (OMIM:613658)
........expandRefsum disease with increased pipecolic acidemia (C535517)
........expandRoifman-Chitayat Syndrome (C567641)
........expandTer Haar syndrome (C537274)
........expandTetra amelia with ectodermal dysplasia and lacrimal duct abnormalities (C536496)
........expandThumbs, Stiff, With Brachydactyly Type A1 And Developmental Delay (C566053)



 Sister Nodes: 
..expandAnxiety, Separation (D001010)
..expandAttention Deficit and Disruptive Behavior Disorders (D019958) Child3
..expandChild Behavior Disorders (D002653) Child1
..expandChild Development Disorders, Pervasive (D002659) Child12
..expandCommunication Disorders (D003147) Child57
..expandDevelopmental Disabilities (D002658) Child39
..expandElimination Disorders (D019960) Child6
..expandFeeding and Eating Disorders of Childhood (D019959)
..expandIntellectual Disability (D008607) Child579
..expandLearning Disorders (D007859) Child12
..expandMotor Skills Disorders (D019957)
..expandMutism (D009155)
..expandReactive Attachment Disorder (D019962)
..expandSchizophrenia, Childhood (D012561)
..expandStereotypic Movement Disorder (D019956) Child1
..expandTic Disorders (D013981) Child3
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:3257
Name:Developmental Disabilities
Definition: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)
Alternative IDs:
ParentIDs:MESH:D019952
TreeNumbers:F03.550.362
Synonyms:Child Development Deviation |Child Development Deviations |Child Development Disorder |Child Development Disorders |Child Development Disorders, Specific |Developmental Delay Disorder |Developmental Delay Disorders |Developmental Disability |Development Deviatio
Slim Mappings:Mental disorder
Reference: MedGen: D002658
MeSH: D002658
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants