failure to thrive
Basic Information
- Description
- A lack of expected normal physiological development in childhood that is characterized by a decelerated or arrested physical growth (height and weight measurements fall below the third or fifth percentile, or a downward change in growth across two major growth percentiles) and is associated with abnormal growth and development.
- Identifier
- SYMP_0000465
- Notation
- SYMP:0000465
- Category
- symptoms
- Database Cross-References
-
- ICD9CM_2005:783.41
- UMLS_CUI:C0015544
- UMLS_ICD9CM_2005_AUI:A0700791
Related Diseases
- ARC syndrome
- Borjeson-Forssman-Lehmann syndrome
- CD3delta deficiency
- CD3epsilon deficiency
- CD3gamma deficiency
- CD3zeta deficiency
- D-glyceric aciduria
- Fanconi anemia
- Fanconi renotubular syndrome 1
- Fanconi renotubular syndrome 3
- Fanconi renotubular syndrome 5
- Fanconi-like syndrome
- Hartnup disease
- Krabbe disease
- MHC class II deficiency
- Marshall syndrome
- Marshall-Smith syndrome
- Nezelof syndrome
- Omenn syndrome
- Pearson syndrome
- Pierson syndrome
- Schuurs-Hoeijmakers Syndrome
- T cell and NK cell immunodeficiency
- T-cell immunodeficiency, congenital alopecia, and nail dystrophy
- TARP syndrome
- TORCH syndrome
- X-linked adrenal hypoplasia congenita
- X-linked reticulate pigmentary disorder
- achalasia microcephaly syndrome
- agammaglobulinemia 8A
- autosomal recessive chronic granulomatous disease 1
- autosomal recessive chronic granulomatous disease 5
- autosomal recessive congenital ichthyosis 4B
- autosomal recessive disease
- autosomal recessive osteopetrosis 5
- autosomal recessive pseudohypoaldosteronism type 1
- brain stem glioma
- cardiofaciocutaneous syndrome
- cerebral creatine deficiency syndrome 1
- childhood acute megakaryoblastic leukemia
- chylomicron retention disease
- combined malonic and methylmalonic acidemia
- combined oxidative phosphorylation deficiency 1
- combined oxidative phosphorylation deficiency 2
- combined oxidative phosphorylation deficiency 37
- combined oxidative phosphorylation deficiency 7
- combined oxidative phosphorylation deficiency 9
- congenital bile acid synthesis defect
- congenital bile acid synthesis defect 1
- congenital bile acid synthesis defect 2
- congenital bile acid synthesis defect 3
- congenital bile acid synthesis defect 5
- congenital diarrhea
- congenital diarrhea 6
- congenital diarrhea 7 with exudative enteropathy
- congenital disorder of glycosylation Ib
- congenital disorder of glycosylation Ic
- congenital disorder of glycosylation Id
- congenital disorder of glycosylation Ie
- congenital disorder of glycosylation Ig
- congenital disorder of glycosylation Ih
- congenital disorder of glycosylation Iu
- congenital disorder of glycosylation Iw
- congenital disorder of glycosylation Ix
- congenital disorder of glycosylation type IIi
- congenital disorder of glycosylation type IIl
- congenital disorder of glycosylation type IIn
- congenital generalized lipodystrophy
- congenital generalized lipodystrophy type 2
- congenital intrinsic factor deficiency
- congenital secretory sodium diarrhea 3
- congenital secretory sodium diarrhea 8
- congenital sucrase-isomaltase deficiency
- craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome
- deafness, dystonia, and cerebral hypomyelination
- dihydropyrimidinase deficiency
- early congenital syphilis
- endocardial fibroelastosis
- endocrine-cerebro-osteodysplasia syndrome
- familial glucocorticoid deficiency
- familial hypobetalipoproteinemia 1
- familial lipoprotein lipase deficiency
- glycine N-methyltransferase deficiency
- homocystinuria-megaloblastic anemia cblE type
- homocystinuria-megaloblastic anemia cblG type
- hypermethioninemia due to adenosine kinase deficiency
- hypervalinemia and hyperleucine-isoleucinemia
- hypobetalipoproteinemia
- hypomyelinating leukodystrophy 3
- immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome
- immunodeficiency 11B
- immunodeficiency 15A
- immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia
- janus kinase-3 deficiency
- juvenile polyposis-hereditary hemorrhagic telangiectasia syndrome
- lambda 5 deficiency
- lissencephaly 1
- lissencephaly 3
- lissencephaly 4
- lissencephaly 5
- lissencephaly 8
- lysinuric protein intolerance
- macrotrabecular hepatoblastoma
- methylmalonic aciduria and homocystinuria type cblC
- methylmalonic aciduria and homocystinuria type cblG
- mitochondrial DNA depletion syndrome 1
- mitochondrial DNA depletion syndrome 11
- mitochondrial DNA depletion syndrome 13
- mitochondrial DNA depletion syndrome 14
- mitochondrial DNA depletion syndrome 15
- mitochondrial DNA depletion syndrome 16
- mitochondrial DNA depletion syndrome 19
- mitochondrial DNA depletion syndrome 8b
- mitochondrial DNA depletion syndrome 9
- mitochondrial complex III deficiency nuclear type 3
- mitochondrial complex IV deficiency nuclear type 16
- mitochondrial complex IV deficiency nuclear type 4
- mitochondrial short-chain enoyl-CoA hydratase 1 deficiency
- multiple mitochondrial dysfunctions syndrome 1
- neuronal intestinal dysplasia type B
- nonphotosensitive trichothiodystrophy 6
- nuclear type mitochondrial complex I deficiency 1
- nuclear type mitochondrial complex I deficiency 11
- obsolete Burkholderia cepacia infectious disease
- obsolete Shwachman-Diamond type metaphyseal dysplasia
- obsolete Tritrichomonadida infectious disease
- obsolete amino acid transport disease
- obsolete apparent mineralocorticoid excess
- obsolete autosomal dominant chronic granulomatous disease
- obsolete cerebral Bilophila wadsworthia infectious disease
- obsolete chronic glomerulonephritis with lesion of membranous glomerulonephritis
- obsolete chronic glomerulonephritis with lesion of proliferative glomerulonephritis
- obsolete congenital muscular dystrophy merosin-positive
- obsolete hypoaldosteronism
- obsolete parasitic stramenopiles infectious disease
- obsolete primary Spirillaceae infectious disease
- orotic aciduria
- otulipenia
- primary autosomal recessive microcephaly 3
- primary hyperoxaluria
- primary hyperoxaluria type 2
- proprotein convertase 1/3 deficiency
- pseudohypoaldosteronism
- pulmonary hemosiderosis
- pyruvate carboxylase deficiency disease
- recombinase activating gene 1 deficiency
- severe combined immunodeficiency with sensitivity to ionizing radiation
- severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive
- severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive
- sialuria
- transcobalamin II deficiency
- transient infantile liver failure
- transient neonatal diabetes mellitus
- trichohepatoenteric syndrome 1
- trichohepatoenteric syndrome 2
- vitamin D-dependent rickets type 1A
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