poor feeding
Basic Information
- Description
- A feeding difficulties and mismanagement that is characterized by an infant with little interest in feeding and it can also refer to an infant who is not feeding enough to receive the necessary nutrition required for adequate growth.
- Identifier
- SYMP_0000355
- Notation
- SYMP:0000355
- Category
- symptoms
Related Diseases
- 3-hydroxyisobutryl-CoA hydrolase deficiency
- 3-methylcrotonyl-CoA carboxylase deficiency
- 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
- Cockayne syndrome B
- White-Sutton syndrome
- X-linked adrenal hypoplasia congenita
- X-linked chronic idiopathic intestinal pseudo-obstruction
- anemia of prematurity
- anomalous left coronary artery from the pulmonary artery
- argininosuccinic aciduria
- combined oxidative phosphorylation deficiency 9
- communicating hydrocephalus
- congenital glutamine deficiency
- congenital heart defects, hamartomas of tongue, and polysyndactyly
- congenital heart disease
- congenital nongoitrous hypothyroidism 4
- familial hyperinsulinemic hypoglycemia 1
- familial hyperinsulinemic hypoglycemia 3
- familial hyperinsulinemic hypoglycemia 8
- galactokinase deficiency
- galactosemia 4
- hypervalinemia and hyperleucine-isoleucinemia
- intestinal botulism
- isovaleric acidemia
- medium chain acyl-CoA dehydrogenase deficiency
- mitochondrial complex IV deficiency nuclear type 15
- neonatal diabetes mellitus with congenital hypothyroidism
- neonatal urinary tract infectious disease
- neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies
- obsolete Diabetes mellitus of mother, with delivery
- obsolete Morganella morganii intestinal infectious disease
- obsolete Picornaviridae infectious disease
- obsolete Zellweger spectrum disorder
- obsolete adrenal hemorrhage of fetus or newborn
- obsolete inborn errors fructose metabolism
- obsolete perinatal infectious disease
- obstructive hydrocephalus
- peroxisome biogenesis disorder 10A
- pontocerebellar hypoplasia type 7
- pyridoxine-dependent epilepsy
- synostosis
- tetanus neonatorum
- tricuspid atresia
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