short stature

short stature, referring to a height of a human being which is below expected

Types

precocious puberty, Proportionate short stature, Disproportionate short stature

Wikipedia Page

http://en.wikipedia.org/wiki/Short_stature

Class

phenomenon, medical condition, symptom, medical concept, disease

Causes

▶ tuberculosis; Down syndrome; cystic fibrosis; tonsillitis; asthma;  …

urinary tract infection; Turner syndrome; celiac disease; hydrocephalus; sickle-cell disease; rickets; Tay-Sachs disease; Diabetes mellitus type 1; Prader-Willi syndrome; enchondromatosis; Kwashiorkor; Williams syndrome; bronchiectasis; Tetralogy of Fallot; Congenital adrenal hyperplasia; chronic renal failure; Osteogenesis imperfecta; cretinism; Cri du chat; Noonan syndrome; Marasmus; Gaucher's disease; Xeroderma pigmentosum; Patent ductus arteriosus; malabsorption; Ascariasis; Maple syrup urine disease; Fanconi anemia; Werner syndrome; Hurler syndrome; pseudopseudohypoparathyroidism; Canavan disease; Hunter syndrome; Bartter syndrome; Wolf-Hirschhorn syndrome; Bardet-Biedl syndrome; CHARGE syndrome; Familial dysautonomia; Septo-optic dysplasia; Menkes disease; Rubinstein-Taybi syndrome; XX male syndrome; cystinosis; Cockayne syndrome; Opitz-Kaveggia syndrome; Ellis-van Creveld syndrome; Cleidocranial dysplasia; Abetalipoproteinemia; Ornithine carbamyltransferase deficiency; Aarskog syndrome; Acrodermatitis enteropathica; I-cell disease; Barth syndrome; Multiple lentigines syndrome; Wolman disease; Pelizaeus-Merzbacher disease; Mowat-Wilson syndrome; Coffin-Lowry syndrome; Donohue syndrome; Progressive familial intrahepatic cholestasis; Albright's hereditary osteodystrophy; Orotic aciduria; Tricho-thiodystrophy; Lysinuric protein intolerance; Geroderma osteodysplastica; Nijmegen breakage syndrome; Fucosidosis; Congenital disorder of glycosylation; Metaphyseal chondrodysplasia, McKusick type; Rapadilino syndrome; Aspartylglucosaminuria; Léri-Weill dyschondrosteosis; Marden-Walker syndrome; hereditary motor and sensory neuropathy; Galactosialidosis; Johanson-Blizzard syndrome; Yunis-Varon syndrome; 3M syndrome; Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome; Hawkinsinuria; Weill-Marchesani syndrome; Mucolipidosis III alpha/beta; Galactose epimerase deficiency; D-Glyceric acidemia; Acromicric dysplasia; SHORT syndrome; 2q37 deletion syndrome; Isobutyryl-coenzyme A dehydrogenase deficiency; Aase-Smith syndrome; Adiposogenital dystrophy; Cutis laxa, autosomal recessive, type 2; Gangliosidosis GM1, type 1; Niemann-Pick disease type B; Carey-Fineman-Ziter syndrome; Tarsal-carpal coalition syndrome; Sutherland-Haan syndrome; Trichorhinophalangeal syndrome type 3; Pitt-Rogers-Danks syndrome; Baller-Gerold syndrome; Systemic infantile hyalinosis; Craniomandibular dermatodysostosis; Otopalatodigital syndrome type 2; Kenny-Caffey-Linarelli syndrome; Watson syndrome; Sanjad-Sakati syndrome; Nephropathic early-onset cystinosis; Silver syndrome; Sexual abuse; Premature labour and/or delivery; MELAS; Complement 5 deficiency; X-linked mental retardation-hypotonic facies syndrome; GRACILE syndrome; Velocardiofacial syndrome; Choledochal cyst; Child abuse; Carbamoylphosphate synthetase deficiency; Adenylosuccinate lyase deficiency; Chylomicron retention disease; Intrauterine growth retardation; Langerhans cell histiocytosis

Related Websites

http://www.height-increasing.com/causes-for-short-stature

Freebase ID

"/guid/9202a8c04000641f80000000006ea4d0"

Diseaseome URI

http://www4.wiwiss.fu-berlin.de/diseasome/resource/diseases/1050

DBPedia URI

http://dbpedia.org/resource/Short_stature

Mesh ID

"D005183"

Diseases DB id

"18756"

Cause

▶ tuberculosis; Down syndrome; cystic fibrosis; tonsillitis; asthma;  …

urinary tract infection; Prednisolone; celiac disease; hydrocephalus; sickle-cell disease; rickets; Tay-Sachs disease; Diabetes mellitus type 1; Prader-Willi syndrome; enchondromatosis; Kwashiorkor; Williams syndrome; bronchiectasis; Tetralogy of Fallot; Congenital adrenal hyperplasia; chronic renal failure; Osteogenesis imperfecta; cretinism; Cri du chat; Marasmus; Gaucher's disease; Xeroderma pigmentosum; Patent ductus arteriosus; malabsorption; Ascariasis; Maple syrup urine disease; Fanconi anemia; Werner syndrome; Hurler syndrome; pseudopseudohypoparathyroidism; Canavan disease; Hunter syndrome; Bartter syndrome; Wolf-Hirschhorn syndrome; Bardet-Biedl syndrome; CHARGE syndrome; Familial dysautonomia; Septo-optic dysplasia; Menkes disease; Rubinstein-Taybi syndrome; XX male syndrome; cystinosis; Cockayne syndrome; Opitz-Kaveggia syndrome; Ellis-van Creveld syndrome; Cleidocranial dysplasia; Abetalipoproteinemia; Ornithine carbamyltransferase deficiency; Aarskog syndrome; Acrodermatitis enteropathica; I-cell disease; Barth syndrome; Multiple lentigines syndrome; Wolman disease; Pelizaeus-Merzbacher disease; Mowat-Wilson syndrome; Coffin-Lowry syndrome; Donohue syndrome; Progressive familial intrahepatic cholestasis; Albright's hereditary osteodystrophy; Orotic aciduria; Tricho-thiodystrophy; Lysinuric protein intolerance; Geroderma osteodysplastica; Nijmegen breakage syndrome; Fucosidosis; Congenital disorder of glycosylation; Metaphyseal chondrodysplasia, McKusick type; Rapadilino syndrome; Aspartylglucosaminuria; Léri-Weill dyschondrosteosis; Marden-Walker syndrome; hereditary motor and sensory neuropathy; Galactosialidosis; Johanson-Blizzard syndrome; Yunis-Varon syndrome; 3M syndrome; Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome; Hawkinsinuria; Weill-Marchesani syndrome; Mucolipidosis III alpha/beta; Galactose epimerase deficiency; D-Glyceric acidemia; Acromicric dysplasia; SHORT syndrome; Bloom syndrome protein; 2q37 deletion syndrome; Isobutyryl-coenzyme A dehydrogenase deficiency; Aase-Smith syndrome; Adiposogenital dystrophy; Cutis laxa, autosomal recessive, type 2; Creatine deficiency syndrome, X-linked; Majeed syndrome; Mucolipidosis III gamma; Methylmalonic acidemia and homocystinuria, cblC type; Mucopolysaccharidosis IX; Gangliosidosis GM1, type 1; S-adenosylhomocysteine hydrolase deficiency; Emanuel syndrome; Niemann-Pick disease type B; Intestinal enteropeptidase deficiency; 3-Hydroxyisobutyric aciduria; Hyperostosis corticalis deformans juvenilis; Crome syndrome; Weismann-Netter-Stuhl syndrome; Carey-Fineman-Ziter syndrome; Tarsal-carpal coalition syndrome; Sutherland-Haan syndrome; De Barsy syndrome; Dwarfism-cerebral atrophy-keratosis follicularis syndrome; Trismus pseudocamptodactyly syndrome; Nonbullous congenital ichthyosiform erythroderma; Aminomethyltransferase deficiency; Glycine decarboxylase deficiency; Trichorhinophalangeal syndrome type 3; Microphthalmia-dermal aplasia-sclerocornea syndrome; Floating-Harbor syndrome; Periodic hyperlysinemia; Pitt-Rogers-Danks syndrome; Filippi syndrome; Baller-Gerold syndrome; Golabi-Ito-Hall syndrome; Systemic infantile hyalinosis; Craniomandibular dermatodysostosis; Otopalatodigital syndrome type 2; Kenny-Caffey-Linarelli syndrome; Martsolf syndrome; Multiple pterygium syndrome; Ramon syndrome; Faciocardiorenal syndrome; Hallermann-Streiff syndrome (HSS); Fryns-van den Berghe syndrome; Neuhauser syndrome; Hurst microtia-absent patellae-micrognathia syndrome; Jeune thoracic dystrophy syndrome; Young-Hughes syndrome; Renpenning syndrome 1; Atkin-Flaitz-Patil syndrome; Chromosome 20 ring syndrome; Deletion of short arm of chromosome 18; Chromosome 15q deletion syndrome; Chromosome 6 ring syndrome; Chromosome 4 ring syndrome; Lenz-Majewski hyperostosis syndrome; Watson syndrome; Kabuki make-up syndrome; Coffin syndrome 1; Carbonic anhydrase type 2 deficiency; Opitz trigonocephaly syndrome; Bonnet-Dechaume-Blanc syndrome; Sanjad-Sakati syndrome; Gangliosidosis GM3; Galactosamine-6-sulfatase deficiency; Glycerol kinase deficiency; Nephropathic early-onset cystinosis; Haemoglobin E disease; Silver syndrome; Pyknodysostosis; Sexual abuse; Russell-Silver dwarfism; Premature labour and/or delivery; MELAS; Complement 5 deficiency; Kartagener syndrome; Beta thalassaemia (heterozygous); Branchio-oculo-facial syndrome; Bowen-Conradi syndrome; BRESHECK syndrome; X-linked mental retardation-hypotonic facies syndrome; GRACILE syndrome; Chromosome 10q deletion syndrome; Velocardiofacial syndrome; Choledochal cyst; Glycogenosis type 1a; Cytotoxic therapeutic agents; Child abuse; Carbamoylphosphate synthetase deficiency; Adenylosuccinate lyase deficiency; Chylomicron retention disease; Intrauterine growth retardation; Langerhans cell histiocytosis

Freebase Primary MID

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