Overview
Feeding problem is a finding that may indicate an underlying health condition requiring clinical evaluation.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Double outlet right ventricle
Frequent (30-79%)
Hecht syndrome
Galactose epimerase deficiency
Very frequent (80-99%)
Killian-Teschler-Nicola syndrome
Frequent (30-79%)
Coffin-Siris syndrome
Very frequent (80-99%)
Acute neuronopathic Gaucher's disease
Frequent (30-79%)
Russell-Silver syndrome
Very frequent (80-99%)
4p partial monosomy syndrome
Frequent (30-79%)
Juvenile nephropathic cystinosis
Very rare (1-4%)
Glutaric aciduria, type 2
Occasional (5-29%)
GTP cyclohydrolase I deficiency
Always present (100%)
Ehlers-Danlos syndrome, hydroxylysine-deficient
Occasional (5-29%)
Homozygous beta thalassemia
Frequent (30-79%)
Polycystic kidney disease, infantile type
Frequent (30-79%)
Leigh's disease
Frequent (30-79%)
Dihydrolipoamide dehydrogenase deficiency
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
Frequent (30-79%)
Trigeminal neuralgia
Frequent (30-79%)
Locked in syndrome
Frequent (30-79%)
Pachyonychia congenita syndrome
Occasional (5-29%)
De Lange syndrome
Frequent (30-79%)
Globoid cell leukodystrophy, late-onset
Occasional (5-29%)
Paramyotonia congenita
Glossopharyngeal neuralgia
Occasional (5-29%)
Smith-Lemli-Opitz syndrome
Always present (100%)
Quick Facts
- SNOMED CT
- 78164000
- UMLS CUI
- C0232466
- Fully Specified Name
- Feeding problem (finding)
- Associated Conditions
- 25
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.