developmental disorder
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Introduction
More general terms
More specific terms
- agenesis
- agenesis of the corpus callosum with mental retardation, ocular coloboma & micrognathia
- amelogenesis imperfecta
- anhidrotic ectodermal dysplasia
- ankyloglossia (tongue tie)
- anophthalmia (microphthalmia 2)
- anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism
- aortic supravalvular stenosis
- aphakia
- Athabaskan brainstem dysgenesis syndrome (Navajo brainstem syndrome)
- autosomal dominant aplasia of lacrimal & salivary glands (ALSG)
- autosomal dominant keratitis
- autosomal dominant syndactyly; nonsyndromic syndactyly
- Barth syndrome
- Bietti's crystalline dystrophy
- bilateral optic nerve hypoplasia/aplasia
- Bosley-Salih-Alorainy syndrome
- bronchopulmonary dysplasia
- buphthalmos
- campomelic dysplasia
- cat-eye syndrome
- CATCH22 syndrome
- caudal duplication anomaly
- cerebro-oculo-facio-skeletal syndrome (COFS); Pena Shokeir 2 syndrome; Cockayne syndrome type 2
- CHARGE syndrome
- coarctation of the aorta
- congenital alcoholism (teratogenic effects of alcoholism)
- congenital amegakaryocytic thrombocytopenia
- congenital anomaly (birth defect)
- congenital cataracts facial dysmorphism & neuropathy syndrome
- Cornelia de Lange syndrome
- Costello syndrome (faciocutaneoskeletal syndrome)
- craniolenticulosutural dysplasia
- craniometaphyseal dysplasia
- cryptophthalmos syndrome (Fraser syndrome)
- cryptorchidism
- deafness with labyrinthine aplasia, microtia & microdontia (LAMM)
- delayed puberty
- developmental bone disorder
- developmental delay
- developmental disorder of aldosterone deficiency
- developmental disorder syndrome (multisystem disorder)
- developmental dyspraxia
- developmental thyroid disease
- dsytonia deafness syndrome; Mohr-Traneberg syndrome; deafness-dystonia-optic atrophy syndrome; X-linked progressive deafness type 1
- Dyggve-Melchior-Clausen syndrome
- ectopia pupillae
- enteroptosis; Glenard's disease
- ethylmalonic encephalopathy
- familial chronic mucocutaneous candidiasis with thyroid disease (CMCT)
- familial deafness
- Farber disease (Farber lipogranulomatosis)
- fibrous dysplasia
- focal cortical dysplasia
- foveal hypoplasia
- Friedreich ataxia
- hemiplegia alterans (alternating hemiplegia)
- hereditary hyperekplexia (Kok disease, startle disease, stiff baby syndrome)
- heterotaxia; heterotaxy; situs ambiguus
- hip dysplasia
- hypoparathyroidism, sensorineural deafness & renal dysplasia (HDR syndrome)
- hypospadius
- hypotrichosis-lymphedema-telangiectasia syndrome
- IGF1 resistance (resistance to insulin-like growth factor 1)
- imperforate hymen
- infantile epileptic encephalopathy
- infantile systemic hyalinosis
- infundibular hypoplasia & hypopituitarism
- intellectual disability; mental retardation
- Jensen syndrome; opticoacoustic nerve atrophy with dementia
- Johanson-Blizzard syndrome (JBS)
- juvenile hyaline fibromatosis
- Legg-Calve-Perthes disease; pseudocoxalgia; avascular necrosis of the hip
- lethal type multiple pterygium syndrome
- long face syndrome; skeletal open bite
- low birth weight infant (preterm infant)
- lymphedema-hypoparathyroidism syndrome
- malformation; dysmorphism
- malrotation of the intestine
- Meckel syndrome
- Meckel's diverticulum (ileal diverticulum)
- metabolic bone disease
- microglossia
- microphthalmia (nanophthalmos)
- Mobius syndrome; congenital facial diplegia; oromandibular-limb hypogenesis
- Muellerian aplasia
- multiple synostoses syndrome
- myoclonic encephalopathy
- nemaline myopathy (rod myopathy)
- neurocristopathy
- nonlethal type multiple pterygium syndrome; Escobar syndrome; Escobar variant multiple pterygium syndrome
- oral-facial-digital syndrome
- osteopetrosis (Albers-Schonberg disease)
- pancreatic agenesis
- Parry-Romberg syndrome (progressive hemifacial atrophy)
- pectus carinatum; pigeon breast; keeled chest
- pectus excavatum
- Pelizaeus-Merzbacher-like disease
- pervasive developmental disorder; autism spectrum disorder (ASD)
- Peters-plus syndrome
- phenytoin teratogenesis
- phocomelia
- pontocerebellar hypoplasia
- popliteal pterygium syndrome
- pseudohypoparathyroidism
- pulmonary hypoplasia
- pyelectasis (pyelectasia)
- rhombencephalosynapsis
- Rubinstein-Taybi syndrome
- Sabjad-Sakati syndrome; hyoparathyroidism-retardation-dysmorphism (HRD)
- Schwartz-Jampel syndrome (SJS1)
- septo-optic dysplasia (de Morsier's syndrome)
- Shprintzen syndrome; velocardiofacial syndrome
- slipped femoral epiphysis
- Smith-Magenis syndrome
- speech-language disorder; specific language impairment; developmental verbal dyspraxia
- split-hand/foot malformation
- stapes ankylosis with broad thumb & toes
- Sturge-Weber syndrome (encephalotrigeminal angiomatosis)
- symphalangism proximal syndrome
- tarsal-carpal coalition syndrome
- tight hymenal ring
- tooth agenesis
- transient erythroblastopenia of childhood
- VACTERL
- van der Woude syndrome (lip-pit syndrome)
- VATER syndrome
- Warburg micro syndrome
- Warburg micro syndrome 4 (WARBM4)
Additional terms
References
- ↑ National Institute of Neurological Disorders and Stroke (NINDS) NINDS Pervasive Developmental Disorders Information Page https://www.ninds.nih.gov/disorders/all-disorders/pervasive-developmental-disorders-information-page
- ↑ Eunice Kennedy Shriver National Institute of Child Health and Human Development Intellectual and Developmental Disabilities (IDDs): Condition Information https://www.nichd.nih.gov/health/topics/idds/conditioninfo/default
- ↑ [No authors listed] Identifying infants and young children with developmental disorders in the medical home: an algorithm for developmental surveillance and screening. Pediatrics. 2006 Jul;118(1):405-20. PMID: https://www.ncbi.nlm.nih.gov/pubmed/16818591