growth disorders

Preferred Label : growth disorders;

MeSH definition : Deviations from the average values for a specific age and sex in any or all of the following: height, weight, skeletal proportions, osseous development, or maturation of features. Included here are both acceleration and retardation of growth.;

MeSH synonym : disorder, growth; growth disorder; Stunted Growth; Growth, Stunted; Stunting; Stuntings;

MeSH annotation : do not confuse with NUTRITION DISORDERS (disorders of assimilating & utilizing nutrients);

Details

Origin ID

D006130;

UMLS CUI

C0018273;

ATC code(s)
- prasterone [ATC Code]
- quinbolone [ATC Code]
Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Currated CISMeF NLP mapping
- growth alteration, nos [SNOMED Notion]
- growth disorder [Radlex concept]
- growth disorder [Disease (Nov.)]
- growth disorders [MedlinePlus Topic]
MedlinePlus topic(s)
- growth disorders [MedlinePlus Topic]
Record concept(s)
- growth disorders [MeSH concept]
Related MeSH Supplementary Concept(s)
- Berk-Tabatznik syndrome [MeSH Supplementary Concept]
- Borjeson-Forssman-Lehmann syndrome [MeSH Supplementary Concept]
- CODAS syndrome [MeSH Supplementary Concept]
- Clark-Baraitser syndrome [MeSH Supplementary Concept]
- GEMSS syndrome [MeSH Supplementary Concept]
- GOMBO syndrome [MeSH Supplementary Concept]
- Goniodysgenesis-Mental Retardation-Short stature syndrome [MeSH Supplementary Concept]
- Hunter-McAlpine syndrome [MeSH Supplementary Concept]
- Insulin-Like growth factor I deficiency [MeSH Supplementary Concept]
- Insulin-Like growth factor I, resistance to [MeSH Supplementary Concept]
- Insulin-Like growth factor I, resistance to, due to increased binding protein [MeSH Supplementary Concept]
- Krause-Kivlin syndrome [MeSH Supplementary Concept]
- LIG4 syndrome [MeSH Supplementary Concept]
- Leri-Weil syndrome [MeSH Supplementary Concept]
- Meier-Gorlin syndrome [MeSH Supplementary Concept]
- Morillo-Cucci passarge syndrome [MeSH Supplementary Concept]
- Rowley-Rosenberg syndrome [MeSH Supplementary Concept]
- SHORT syndrome [MeSH Supplementary Concept]
- Vater-Like defects with pulmonary hypertension, laryngeal webs, and growth deficiency [MeSH Supplementary Concept]
- acrocapitofemoral dysplasia [MeSH Supplementary Concept]
- acrocephalopolydactylous dysplasia [MeSH Supplementary Concept]
- acromegaloid features, overgrowth, cleft palate, and hernia [MeSH Supplementary Concept]
- agonadism, XY, with mental retardation, short stature, retarded bone age, and multiple extragenital malformations [MeSH Supplementary Concept]
- al gazali khidr prem chandran syndrome [MeSH Supplementary Concept]
- aphalangia syndactyly microcephaly [MeSH Supplementary Concept]
- auriculoosteodysplasia [MeSH Supplementary Concept]
- bellini chiumello rimoldi syndrome [MeSH Supplementary Concept]
- bhaskar jagannathan syndrome [MeSH Supplementary Concept]
- blepharophimosis with ptosis, syndactyly, and short stature [MeSH Supplementary Concept]
- boudhina yedes khiari syndrome [MeSH Supplementary Concept]
- cantalamessa baldini ambrosi syndrome [MeSH Supplementary Concept]
- cantu Sanchez-Corona fragoso syndrome [MeSH Supplementary Concept]
- cataracts, ataxia, short stature, and mental retardation [MeSH Supplementary Concept]
- cataracts, congenital, with sensorineural deafness, down Syndrome-Like facial appearance, short stature, and mental retardation [MeSH Supplementary Concept]
- chitty hall baraitser syndrome [MeSH Supplementary Concept]
- chromosome 15q26-Qter deletion syndrome [MeSH Supplementary Concept]
- chromosome 18 pericentric inversion [MeSH Supplementary Concept]
- coffin syndrome 1 [MeSH Supplementary Concept]
- contractures ectodermal dysplasia cleft lip palate [MeSH Supplementary Concept]
- cote katsantoni syndrome [MeSH Supplementary Concept]
- coxoauricular syndrome [MeSH Supplementary Concept]
- craniofacial abnormalities, cataracts, congenital heart disease, sacral neural tube defects, and growth and developmental retardation [MeSH Supplementary Concept]
- creases, Infra-Auricular cutaneous, with tall stature and advanced bone age [MeSH Supplementary Concept]
- crumpled helices and small mouth [MeSH Supplementary Concept]
- curatolo cilio pessagno syndrome [MeSH Supplementary Concept]
- daish hardman lamont syndrome [MeSH Supplementary Concept]
- dermoids of cornea [MeSH Supplementary Concept]
- devriendt syndrome [MeSH Supplementary Concept]
- dubowitz syndrome [MeSH Supplementary Concept]
- dyschondrosteosis and nephritis [MeSH Supplementary Concept]
- epithelial squamous dysplasia, keratinizing desquamative, of urinary tract [MeSH Supplementary Concept]
- extrasystoles, multiform ventricular, with short stature, hyperpigmentation and microcephaly [MeSH Supplementary Concept]
- fallot complex with severe mental and growth retardation [MeSH Supplementary Concept]
- filippi syndrome [MeSH Supplementary Concept]
- floating-harbor syndrome [MeSH Supplementary Concept]
- frias syndrome [MeSH Supplementary Concept]
- game friedman paradice syndrome [MeSH Supplementary Concept]
- gay feinmesser cohen syndrome [MeSH Supplementary Concept]
- gomez lopez hernandez syndrome [MeSH Supplementary Concept]
- gonadal dysgenesis, hypergonadotropic, XX type, short stature, and recurrent metabolic acidosis [MeSH Supplementary Concept]
- growth and developmental retardation, ocular ptosis, cardiac defect, and anal atresia [MeSH Supplementary Concept]
- growth deficiency and mental retardation with facial dysmorphism [MeSH Supplementary Concept]
- growth failure, microcephaly, mental retardation, cataracts, large joint contractures, osteoporosis, cortical dysplasia, and cerebellar atrophy [MeSH Supplementary Concept]
- growth mental deficiency syndrome of myhre [MeSH Supplementary Concept]
- growth retardation, alopecia, pseudoanodontia and optic atrophy [MeSH Supplementary Concept]
- growth retardation, small and puffy hands and feet, and eczema [MeSH Supplementary Concept]
- hairy elbows [MeSH Supplementary Concept]
- heme oxygenase 1 deficiency [MeSH Supplementary Concept]
- hersh podruch weisskopk syndrome [MeSH Supplementary Concept]
- hooft disease [MeSH Supplementary Concept]
- hutterite cerebroosteonephrodysplasia syndrome [MeSH Supplementary Concept]
- hypoparathyroidism-retardation-dysmorphism syndrome [MeSH Supplementary Concept]
- johanson blizzard syndrome [MeSH Supplementary Concept]
- jorgenson lenz syndrome [MeSH Supplementary Concept]
- kozlowski rafinski klicharska syndrome [MeSH Supplementary Concept]
- kuster majewski hammerstein syndrome [MeSH Supplementary Concept]
- ladda zonana ramer syndrome [MeSH Supplementary Concept]
- langer mesomelic dysplasia [MeSH Supplementary Concept]
- laryngotracheal stenosis, progressive, with short stature and arthropathy [MeSH Supplementary Concept]
- leukomelanoderma, infantilism, mental retardation, hypodontia, hypotrichosis [MeSH Supplementary Concept]
- lipodystrophy, generalized, with mental retardation, deafness, short stature, and slender bones [MeSH Supplementary Concept]
- lowry maclean syndrome [MeSH Supplementary Concept]
- lowry wood syndrome [MeSH Supplementary Concept]
- macrosomia adiposa congenita [MeSH Supplementary Concept]
- madelung deformity [MeSH Supplementary Concept]
- malocclusion and short stature [MeSH Supplementary Concept]
- megarbane syndrome [MeSH Supplementary Concept]
- mental and growth retardation with amblyopia [MeSH Supplementary Concept]
- mental retardation mietens weber type [MeSH Supplementary Concept]
- mental retardation with optic atrophy, facial dysmorphism, microcephaly, and short stature [MeSH Supplementary Concept]
- mental retardation, X-Linked, with short stature [MeSH Supplementary Concept]
- mental retardation, microcephaly, growth retardation, joint contractures, and facial dysmorphism [MeSH Supplementary Concept]
- mental retardation-hypotonic facies syndrome, x-linked, 1 [MeSH Supplementary Concept]
- microcephaly cervical spine fusion anomalies [MeSH Supplementary Concept]
- microdontia hypodontia short stature [MeSH Supplementary Concept]
- milner khallouf gibson syndrome [MeSH Supplementary Concept]
- mitochondrial myopathy with lactic acidosis [MeSH Supplementary Concept]
- mollica pavone antener syndrome [MeSH Supplementary Concept]
- myelodysplasia, immunodeficiency, facial dysmorphism, short stature, and psychomotor delay [MeSH Supplementary Concept]
- nathalie syndrome [MeSH Supplementary Concept]
- neurofaciodigitorenal syndrome [MeSH Supplementary Concept]
- nijmegen breakage Syndrome-Like disorder [MeSH Supplementary Concept]
- omodysplasia type 1 [MeSH Supplementary Concept]
- onat syndrome [MeSH Supplementary Concept]
- osteolysis syndrome recessive [MeSH Supplementary Concept]
- partington anderson syndrome [MeSH Supplementary Concept]
- pectus excavatum, macrocephaly, short stature, dysplastic nails [MeSH Supplementary Concept]
- pfeiffer kapferer syndrome [MeSH Supplementary Concept]
- pfeiffer mayer syndrome [MeSH Supplementary Concept]
- pfeiffer palm teller syndrome [MeSH Supplementary Concept]
- pili torti developmental delay neurological abnormalities [MeSH Supplementary Concept]
- pilotto syndrome [MeSH Supplementary Concept]
- polydysspondyly [MeSH Supplementary Concept]
- premature aging, okamoto type [MeSH Supplementary Concept]
- progeria short stature pigmented nevi [MeSH Supplementary Concept]
- progeroid syndrome, congenital, petty type [MeSH Supplementary Concept]
- qazi markouizos syndrome [MeSH Supplementary Concept]
- radioulnar synostosis retinal pigment abnormalities [MeSH Supplementary Concept]
- ramon syndrome [MeSH Supplementary Concept]
- reardon wilson cavanagh syndrome [MeSH Supplementary Concept]
- renal tubular acidosis, distal, with nephrocalcinosis, short stature, mental retardation, and distinctive facies [MeSH Supplementary Concept]
- rhizomelic dysplasia, scoliosis, and retinitis pigmentosa [MeSH Supplementary Concept]
- rodrigues blindness [MeSH Supplementary Concept]
- rommen mueller sybert syndrome [MeSH Supplementary Concept]
- say meyer syndrome [MeSH Supplementary Concept]
- say syndrome [MeSH Supplementary Concept]
- schaap taylor baraitser syndrome [MeSH Supplementary Concept]
- schimke X-linked mental retardation syndrome [MeSH Supplementary Concept]
- seemanova lesny syndrome [MeSH Supplementary Concept]
- severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation [MeSH Supplementary Concept]
- short stature syndrome, brussels type [MeSH Supplementary Concept]
- short stature, facial dysmorphism, severe brachydactyly, and syndactyly [MeSH Supplementary Concept]
- short stature, idiopathic, X-Linked [MeSH Supplementary Concept]
- slavotinek pike mills hurst syndrome [MeSH Supplementary Concept]
- sonoda syndrome [MeSH Supplementary Concept]
- spastic paraplegia 9, autosomal dominant [MeSH Supplementary Concept]
- spondyloepimetaphyseal dysplasia, pakistani type [MeSH Supplementary Concept]
- spondylometaphyseal dysplasia, 'corner fracture' type [MeSH Supplementary Concept]
- stern lubinsky durrie syndrome [MeSH Supplementary Concept]
- synostosis of talus and calcaneus with short stature [MeSH Supplementary Concept]
- theodor hertz goodman syndrome [MeSH Supplementary Concept]
- thrombocytopenia robin sequence [MeSH Supplementary Concept]
- thumb agenesis, short stature, and immunodeficiency [MeSH Supplementary Concept]
- thumb, hypoplastic, with choroid coloboma, poorly developed antihelix, and deafness [MeSH Supplementary Concept]
- tonoki syndrome [MeSH Supplementary Concept]
- tsukahara syndrome [MeSH Supplementary Concept]
- vertebral body fusion overgrowth [MeSH Supplementary Concept]
- viljoen kallis voges syndrome [MeSH Supplementary Concept]
- volcke soekarman syndrome [MeSH Supplementary Concept]
- wellesley carmen french syndrome [MeSH Supplementary Concept]
- wiedemann grosse dibbern syndrome [MeSH Supplementary Concept]
- winchester syndrome [MeSH Supplementary Concept]
- wittwer syndrome [MeSH Supplementary Concept]
- young hughes syndrome [MeSH Supplementary Concept]
- zerres rietschel majewski syndrome [MeSH Supplementary Concept]
- zinc deficiency, neonatal, due to low breast milk zinc [MeSH Supplementary Concept]
See also
- bone diseases, developmental [MeSH Descriptor]
- dwarfism [MeSH Descriptor]
- gigantism [MeSH Descriptor]
See also (suggested by CISMeF)
- failure to thrive [MeSH Descriptor]
- growth [MeSH Descriptor]
Semantic type(s)
- Pathologic Function [UMLS semantic type]
UMLS correspondences (same concept)
- Growth disorder [MedDRA Preferred Term]
- growth disorder [Radlex concept]
- growth disorders [MedlinePlus Topic]

Keyword's position in hierarchy(ies) :

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