short stature
Basic Information
- Description
- A lack of expected normal physiological development in childhood that is characterized by an individual's height being in the 3rd percentile for the mean height of a given age, sex, and population group.
- Identifier
- SYMP_0000568
- Notation
- SYMP:0000568
- Category
- symptoms
- Database Cross-References
-
- ICD9CM_2005:783.43
- UMLS_CUI:C0349588
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- 3-methylglutaconic aciduria type 1
- 3MC syndrome 3
- AMED syndrome
- Aarskog syndrome
- Albright's hereditary osteodystrophy
- Armfield syndrome
- Baraitser-Winter syndrome
- Baraitser-Winter syndrome 1
- Baraitser-Winter syndrome 2
- Bardet-Biedl syndrome 20
- Bruck syndrome
- Cockayne syndrome
- Cockayne syndrome A
- Cockayne syndrome B
- Coffin-Siris syndrome
- Coffin-Siris syndrome 1
- Coffin-Siris syndrome 10
- Coffin-Siris syndrome 4
- Coffin-Siris syndrome 6
- Coffin-Siris syndrome 7
- Coffin-Siris syndrome 8
- Coffin-Siris syndrome 9
- Cohen syndrome
- Cornelia de Lange syndrome 1
- Culler-Jones syndrome
- De Sanctis-Cacchione syndrome
- Desbuquois dysplasia
- Dubowitz syndrome
- Dyggve-Melchior-Clausen disease
- Ehlers-Danlos syndrome spondylodysplastic type 1
- Ehlers-Danlos syndrome spondylodysplastic type 2
- Ehlers-Danlos syndrome spondylodysplastic type 3
- Ellis-Van Creveld syndrome
- Fanconi anemia
- Fanconi anemia complementation group A
- Fanconi anemia complementation group B
- Fanconi anemia complementation group C
- Fanconi anemia complementation group D2
- Fanconi anemia complementation group E
- Fanconi anemia complementation group F
- Fanconi anemia complementation group G
- Fanconi anemia complementation group I
- Fanconi anemia complementation group J
- Fanconi anemia complementation group N
- Fanconi anemia complementation group P
- Fanconi anemia complementation group Q
- Fanconi anemia complementation group R
- Fanconi anemia complementation group T
- Fanconi anemia complementation group U
- Fanconi syndrome
- Floating-Harbor syndrome
- Hajdu-Cheney syndrome
- Jacobsen Syndrome
- Jansen's metaphyseal chondrodysplasia
- Johanson-Blizzard syndrome
- Joubert syndrome 2
- Kallmann syndrome
- Kaufman oculocerebrofacial syndrome
- Kenny-Caffey syndrome
- Kenny-Caffey syndrome type 1
- Kenny-Caffey syndrome type 2
- King Denborough syndrome
- Kniest dysplasia
- Larsen-like syndrome B3GAT3 type
- Laurence-Moon syndrome
- Leri-Weill dyschondrosteosis
- MERRF syndrome
- Marinesco-Sjogren syndrome
- Marshall syndrome
- Marshall-Smith syndrome
- Meier-Gorlin syndrome
- Meier-Gorlin syndrome 1
- Meier-Gorlin syndrome 2
- Meier-Gorlin syndrome 3
- Meier-Gorlin syndrome 4
- Meier-Gorlin syndrome 5
- Meier-Gorlin syndrome 6
- Meier-Gorlin syndrome 7
- Meier-Gorlin syndrome 8
- Melnick-Needles syndrome
- Mullegama-Klein-Martinez syndrome
- Nicolaides-Baraitser syndrome
- Noonan syndrome
- Noonan syndrome 1
- Noonan syndrome 10
- Noonan syndrome 11
- Noonan syndrome 12
- Noonan syndrome 2
- Noonan syndrome 3
- Noonan syndrome 4
- Noonan syndrome 5
- Noonan syndrome 6
- Noonan syndrome 7
- Noonan syndrome 8
- Noonan syndrome 9
- Noonan syndrome with multiple lentigines
- Noonan syndrome with multiple lentigines 1
- Noonan syndrome with multiple lentigines 2
- Noonan syndrome with multiple lentigines 3
- Noonan syndrome-like disorder with loose anagen hair
- Noonan syndrome-like disorder with loose anagen hair 1
- Peters plus syndrome
- Renpenning syndrome
- Robinow syndrome
- Ruijs-Aalfs syndrome
- SADDAN
- SHORT syndrome
- SHOX-related short stature
- Saul-Wilson syndrome
- Schimke immuno-osseous dysplasia
- Schmid metaphyseal chondrodysplasia
- Schwartz-Jampel syndrome 1
- Shwachman-Diamond syndrome
- Sifrim-Hitz-Weiss syndrome
- Silver-Russell syndrome
- Sjogren-Larsson syndrome
- Smith-McCort dysplasia
- Smith-McCort dysplasia 2
- Stickler syndrome 1
- Stickler syndrome 2
- Stocco Dos Santos type X-linked intellectual disability
- Sweeney-Cox syndrome
- Troyer syndrome
- Turner syndrome
- Van Esch-O'Driscoll syndrome
- Watson syndrome
- Weill-Marchesani syndrome
- Weissenbacher-Zweymuller syndrome
- White-Sutton syndrome
- Williams-Beuren syndrome
- Wilson-Turner syndrome
- X-linked chondrodysplasia punctata 1
- X-linked chondrodysplasia punctata 2
- X-linked deafness 5
- X-linked dominant disease
- X-linked dominant hypophosphatemic rickets
- X-linked spondyloepimetaphyseal dysplasia
- X-linked spondyloepiphyseal dysplasia tarda
- Xia-Gibbs Syndrome
- Y-linked spermatogenic failure 1
- ZTTK syndrome
- Zaki syndrome
- achondroplasia
- acrocapitofemoral dysplasia
- acrodysostosis
- acrofacial dysostosis, Catania type
- acromesomelic dysplasia
- acromesomelic dysplasia, Grebe type
- acromesomelic dysplasia, Hunter-Thompson type
- acromesomelic dysplasia-4
- acromicric dysplasia
- alpha thalassemia-X-linked intellectual disability syndrome
- anauxetic dysplasia 2
- autosomal dominant Aarskog syndrome
- autosomal dominant Robinow syndrome 1
- autosomal dominant Robinow syndrome 2
- autosomal dominant chondrodysplasia punctata
- autosomal dominant craniodiaphyseal dysplasia
- autosomal dominant dyskeratosis congenita 3
- autosomal dominant dyskeratosis congenita 4
- autosomal dominant hypophosphatemic rickets
- autosomal dominant spondyloepiphyseal dysplasia tarda
- autosomal recessive Robinow syndrome
- autosomal recessive Robinow syndrome 2
- autosomal recessive congenital ichthyosis 4B
- autosomal recessive hypophosphatemic rickets
- autosomal recessive spondyloepiphyseal dysplasia tarda Leroy-Spranger type
- axial spondylometaphyseal dysplasia
- brachycephaly, trichomegaly, and developmental delay
- brachydactyly type A6
- brachydactyly type E1
- brachydactyly type E2
- brachyolmia
- brachyolmia-amelogenesis imperfecta syndrome
- cartilage-hair hypoplasia
- cerebellar ataxia, mental retardation and dysequlibrium syndrome
- childhood hypophosphatasia
- chondrodysplasia with joint dislocations gPAPP type
- chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia
- chondrodysplasia-pseudohermaphroditism syndrome
- chromosome 16p11.2 duplication syndrome
- chromosome 16p12.2-p11.2 deletion syndrome
- chromosome 16q22 deletion syndrome
- chromosome 17q21.31 duplication syndrome
- chromosome 17q23.1-q23.2 deletion syndrome
- chromosome 18p deletion syndrome
- chromosome 18q deletion syndrome
- chromosome 1q21.1 deletion syndrome
- chromosome 1q21.1 duplication syndrome
- chromosome 1q41-q42 deletion syndrome
- chromosome 2p12-p11.2 deletion syndrome
- chromosome 2q31.2 deletion syndrome
- chromosome 2q37 deletion syndrome
- chromosome 5q12 deletion syndrome
- classic galactosemia
- cleidocranial dysplasia
- combined oxidative phosphorylation deficiency 55
- congenital disorder of glycosylation Ia
- congenital disorder of glycosylation Id
- congenital disorder of glycosylation In
- congenital disorder of glycosylation Iw
- congenital disorder of glycosylation type I
- congenital disorder of glycosylation type II
- congenital disorder of glycosylation type IIc
- congenital disorder of glycosylation type IIf
- congenital disorder of glycosylation type IIp
- congenital dyserythropoietic anemia type II
- congenital dyserythropoietic anemia type Ia
- congenital dyserythropoietic anemia type Ib
- congenital nongoitrous hypothyroidism 9
- contractures, pterygia, and spondylocarpotarsal fusion syndrome
- contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A
- contractures, pterygia, and spondylocarpotarsal fusion syndrome 1B
- craniodiaphyseal dysplasia
- cranioectodermal dysplasia 3
- craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome
- dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome
- diphthamide deficiency syndrome 1
- diphthamide deficiency syndrome 2
- distal arthrogryposis type 3
- familial hyperinsulinemic hypoglycemia 2
- familial hyperinsulinemic hypoglycemia 6
- fibrochondrogenesis
- fibrochondrogenesis 1
- fibrochondrogenesis 2
- galactosialidosis
- geleophysic dysplasia
- geleophysic dysplasia 2
- glycogen storage disease IXb
- glycosylphosphatidylinositol biosynthesis defect 16
- growth hormone insensitivity syndrome with immune dysregulation 2
- hereditary hypophosphatemic rickets with hypercalciuria
- hereditary lymphedema I
- hereditary lymphedema ID
- hereditary lymphedema II
- hereditary spastic paraplegia 47
- hereditary spastic paraplegia 54
- hereditary spastic paraplegia 87
- hereditary spastic paraplegia 9B
- hypertension and brachydactyly syndrome
- hypochondroplasia
- hypogonadotropic hypogonadism 16 with or without anosmia
- hypogonadotropic hypogonadism 3 with or without anosmia
- hypophosphatasia
- hypophosphatemic nephrolithiasis/osteoporosis 2
- intellectual developmental disorder with abnormal behavior, microcephaly, and short stature
- intellectual developmental disorder with short stature and behavioral abnormalities
- isolated growth hormone deficiency
- isolated growth hormone deficiency type IB
- isolated growth hormone deficiency type III
- linear skin defects with multiple congenital anomalies 1
- linear skin defects with multiple congenital anomalies 3
- lipid metabolism disorder
- lysinuric protein intolerance
- mandibulofacial dysostosis, Guion-Almeida type
- metaphyseal dysplasia-maxillary hypoplasia-brachydactyly syndrome
- metatropic dysplasia
- microcephaly, growth deficiency, seizures, and brain malformations
- microcephaly, seizures, and developmental delay
- microcephaly, short stature, and limb abnormalities
- mitochondrial complex IV deficiency nuclear type 15
- mosaic variegated aneuploidy syndrome
- mucolipidosis III gamma
- mucopolysaccharidosis
- mucopolysaccharidosis IV
- mucopolysaccharidosis Ih/s
- mucopolysaccharidosis VI
- mucopolysaccharidosis type IVB
- multiple benign circumferential skin creases on limbs
- multiple epiphyseal dysplasia 1
- multiple epiphyseal dysplasia 2
- multiple epiphyseal dysplasia 3
- multiple epiphyseal dysplasia 7
- multiple epiphyseal dysplasia due to collagen 9 anomaly
- myopathy, lactic acidosis, and sideroblastic anemia
- neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties
- neurodevelopmental disorder with spastic paraplegia and microcephaly
- neurofibromatosis 1
- neurofibromatosis-Noonan syndrome
- nonphotosensitive trichothiodystrophy 4
- oblique facial clefting 1
- obsolete Jensen syndrome
- obsolete Majewski syndrome
- obsolete McKusick type metaphyseal dysplasia
- obsolete Noonan syndrome 1
- obsolete Noonan syndrome 10
- obsolete Noonan syndrome 2
- obsolete Noonan syndrome 3
- obsolete Noonan syndrome 4
- obsolete Noonan syndrome 5
- obsolete Noonan syndrome 6
- obsolete Noonan syndrome 7
- obsolete Peters-Plus Syndrome
- obsolete Saldino-Noonan syndrome
- obsolete Shwachman-Diamond type metaphyseal dysplasia
- obsolete Verma-Naumoff syndrome
- obsolete X-linked sensorineural deafness
- obsolete apparent mineralocorticoid excess
- obsolete congenital disorder of glycosylation type 2m
- obsolete familial hypophosphatemia
- obsolete lentiginosis profusa
- obsolete metastatic osteosarcoma
- obsolete trichorhinophalangeal syndrome I
- omodysplasia
- omodysplasia 1
- orofaciodigital syndrome VIII
- orofaciodigital syndrome XVIII
- osteochondrodysplasia
- osteogenesis imperfecta
- osteogenesis imperfecta type 1
- osteogenesis imperfecta type 11
- osteogenesis imperfecta type 12
- osteogenesis imperfecta type 13
- osteogenesis imperfecta type 14
- osteogenesis imperfecta type 15
- osteogenesis imperfecta type 16
- osteogenesis imperfecta type 17
- osteogenesis imperfecta type 18
- osteogenesis imperfecta type 2
- osteogenesis imperfecta type 20
- osteogenesis imperfecta type 3
- osteogenesis imperfecta type 5
- osteogenesis imperfecta type 9
- osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures
- osteosclerotic metaphyseal dysplasia
- otopalatodigital syndrome type 1
- ovarian dysgenesis 4
- photosensitive trichothiodystrophy
- photosensitive trichothiodystrophy 1
- photosensitive trichothiodystrophy 2
- poikiloderma with neutropenia
- popliteal pterygium syndrome
- primary autosomal recessive microcephaly
- primary autosomal recessive microcephaly 1
- primary autosomal recessive microcephaly 10
- primary autosomal recessive microcephaly 11
- primary autosomal recessive microcephaly 12
- primary autosomal recessive microcephaly 13
- primary autosomal recessive microcephaly 14
- primary autosomal recessive microcephaly 15
- primary autosomal recessive microcephaly 16
- primary autosomal recessive microcephaly 19
- primary autosomal recessive microcephaly 6
- primary autosomal recessive microcephaly 7
- primary autosomal recessive microcephaly 9
- primary ciliary dyskinesia
- primary microcephaly
- progeroid syndrome
- progressive familial intrahepatic cholestasis 1
- pseudohypoparathyroidism type IB
- pycnodysostosis
- rapadilino syndrome
- renal coloboma syndrome
- schneckenbecken dysplasia
- selective pituitary thyroid hormone resistance
- septooptic dysplasia
- short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies
- short stature, hearing loss, retinitis pigmentosa, and distinctive facies
- short-rib thoracic dysplasia 11 with or without polydactyly
- short-rib thoracic dysplasia 18 with polydactyly
- short-rib thoracic dysplasia 7 with or without polydactyly
- solitary median maxillary central incisor
- split hand-foot malformation 2
- spondylocostal dysostosis
- spondylocostal dysostosis 6
- spondyloepimetaphyseal dysplasia
- spondyloepimetaphyseal dysplasia with joint laxity
- spondyloepimetaphyseal dysplasia with joint laxity type 2
- spondyloepimetaphyseal dysplasia with joint laxity type 3
- spondyloepimetaphyseal dysplasia, Genevieve-type
- spondyloepimetaphyseal dysplasia, Pakistani type
- spondyloepimetaphyseal dysplasia, Sponastrime type
- spondyloepimetaphyseal dysplasia, Strudwick type
- spondyloepiphyseal dysplasia
- spondyloepiphyseal dysplasia Kimberley type
- spondyloepiphyseal dysplasia Maroteaux type
- spondyloepiphyseal dysplasia Nishimura type
- spondyloepiphyseal dysplasia Stanescu type
- spondyloepiphyseal dysplasia tarda
- spondyloepiphyseal dysplasia tarda with characteristic facies
- spondyloepiphyseal dysplasia tarda with intellectual disability
- spondyloepiphyseal dysplasia with congenital joint dislocations
- spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and intellectual disability
- spondyloepiphyseal dysplasia with punctate corneal dystrophy
- spondyloepiphyseal dysplasia-brachydactyly and distinctive speech
- spondylometaphyseal dysplasia
- spondylometaphyseal dysplasia Algerian type
- spondylometaphyseal dysplasia East African type
- spondylometaphyseal dysplasia Kozlowski type
- spondylometaphyseal dysplasia Megarbane-Dagher-Melike type
- spondylometaphyseal dysplasia corner fracture type
- spondylometaphyseal dysplasia type A4
- spondylometaphyseal dysplasia with bowed forearms and facial dysmorphism
- spondylometaphyseal dysplasia with corneal dystrophy
- spondyloperipheral dysplasia
- stiff skin syndrome
- syndromic X-linked intellectual disability Cabezas type
- syndromic X-linked intellectual disability Claes-Jensen type
- syndromic X-linked intellectual disability Raymond type
- syndromic X-linked intellectual disability Turner type
- syndromic microphthalmia
- syndromic microphthalmia 13
- syndromic microphthalmia 5
- syndromic microphthalmia 6
- thiamine-responsive megaloblastic anemia syndrome
- thyroid hormone resistance syndrome
- trichohepatoenteric syndrome
- trichorhinophalangeal syndrome type II
- trichorhinophalangeal syndrome type III
- trichothiodystrophy
- ulnar-mammary syndrome
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