Disease Index
9,486 diseasesinfantile-onset ascending hereditary spastic paralysis
Infantile-onset ascending hereditary spastic paralysis (IAHSP) is a very rare motor neuron disease characterized by severe spasticity of the lower limbs in early life, progression of spasticity to the upper limbs in late childhood, and dysarthria
ICD: G12.2MeSH: C537217
infantile-onset autosomal recessive nonprogressive cerebellar ataxia
human disease
MeSH: C537312
infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome
human disease
infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
human disease
infantile-onset X-linked spinal muscular atrophy
MeSH: C535380
infectious anterior uveitis
Human disease
infectious disease of the nervous system
infectious disease that involves the nervous system
infectious disease with dementia
human disease
infectious disease with epilepsy
human disease
infectious disease with peripheral neuropathy
human disease
infectious embryofetopathy
human disease
infectious encephalitis
brain inflammation caused by an infectious agent
MeSH: D000069544
infectious epithelial keratitis
human disease
infectious myositis
human disease
infectious panuveitis
human disease
infectious posterior uveitis
human disease
infective dermatitis associated with HTLV-1
inferior vena cava interruption
human disease
inflammatory and autoimmune disease with epilepsy
human disease
inflammatory bowel disease 21
inflammatory bowel disease that has material basis in variation in the chromosome region 18p11
MeSH: C567338
inflammatory bowel diseases
intestinal disease characterized by inflammation located in all parts of digestive tract
MeSH: D015212
Inflammatory linear verrucous epidermal nevus
human disease
inflammatory myofibroblastic tumour
mesenchymal cell neoplasm that has material basis in myofibroblastic cells admixed with inflammatory cells
inflammatory myopathy with abundant macrophages
human disease
infundibulo-neurohypophysitis
human disease
infundibulopelvic stenosis-multicystic kidney syndrome
MeSH: C535528
inhalation anthrax
human disease
ICD: A22.1
inhalational botulism
Inhalational botulism is a man-made form of botulism (see this term), a rare acquired neuromuscular junction disease with descending flaccid paralysis caused by botulinum neurotoxins (BoNTs)
inherited acute myeloid leukemia
instance of acute myeloid leukemia that is caused by an inherited modification of the individual's genome
inherited blood coagulation disease
Human disease
MeSH: D025861