Disease Index
9,486 diseasesinborn disorder of pentose phosphate metabolism
human disease
inborn disorder of peptide metabolism
human disease
inborn disorder of phenylalanine or tyrosine metabolism
human disease
inborn disorder of porphyrin and haem metabolism
acquired metabolic disease that is has its basis in the disruption of porphyrin-containing compound metabolic process
inborn disorder of purine metabolism
acquired metabolic disease that is has its basis in the disruption of purine nucleobase metabolic process
inborn disorder of serine or glycine metabolism
human disease
inborn disorder of the gamma-glutamyl cycle
human disease
inborn error of lipid metabolism
medical condition
MeSH: D008052
inborn errors of purine–pyrimidine metabolism
inherited metabolic disorder involving dysfunction of purine and pyrimidine metabolism
MeSH: D011686
incessant infant ventricular tachycardia
incisors, lower central, absence of
human disease
inclusion body myopathy with Paget disease of bone and frontotemporal dementia
syndrome
ICD: G71.8
inclusion body myositis
inflammatory muscle disease in older adults
MeSH: D018979
inclusion myopathy
human disease
inclusion-cell disease
Human disease
ICD: E77.0MeSH: C538602
incontinentia pigmenti achromians
Human disease
ICD: L81.6
Indeterminate cell histiocytosis
human disease
indeterminate colitis
human disease
Indian tick typhus
Human disease
indolent B-cell non-Hodgkin lymphoma
human disease
indolent primary cutaneous B-cell lymphoma
human disease
indolent primary cutaneous T-cell lymphoma
human disease
indolent systemic mastocytosis
human disease
ICD: D47.0
indomethacin embryofetopathy
infancy electroclinical syndrome
electroclinical syndrome with onset in infancy occurring between birth and one year of age
infant botulism
Human disease
infant epilepsy with migrant focal crisis
infant respiratory distress syndrome
human disease affecting newborns
MeSH: D006819
infantile apnea
medical condition
infantile axonal neuropathy
human disease