Disease Index

9,486 diseases
Acropectoral syndrome
medical condition
MeSH: C535664
acropectororenal dysplasia
acropectorovertebral dysplasia
MeSH: C566319
acropustulosis
Human disease
acrorenal syndrome
Human disease
MeSH: C563159
acryocystitis-osteopoikilosis syndrome
ICD: H04.3MeSH: C536061
ACTH-dependent Cushing syndrome
ACTH-independent Cushing syndrome
ACTH-independent Cushing syndrome due to rare cortisol-producing adrenal tumor
human disease
actinic lichen planus
Actinic lichen planus (LP) is a rare variant of cutaneous lichen planus (see this term) characterized by the development of photo-distributed lichenoid lesions
actinic prurigo
rare sunlight-induced, pruritic, papular or nodular skin eruption
MeSH: C566780
actinomycosis
Human disease
MeSH: D000196
activated PI3K delta syndrome
medical condition
acute and subacute inflammatory demyelinating polyneuropathy
human disease
acute annular outer retinopathy
human disease
acute basophilic leukemia
rare acute myeloid leukemia in which the immature cells differentiate towards basophils
MeSH: D015471
acute biphenotypic leukaemia
uncommon type of leukemia which arises in multipotent progenitor cells which have the ability differentiating into both myeloid and lymphoid lineages
MeSH: D015456
acute disseminated encephalomyelitis
encephalomyelitis characterized by inflammation located in brain and located in spinal cord that damages myelin
MeSH: D004673
acute encephalopathy with biphasic seizures and late reduced diffusion
human disease
acute encephalopathy with inflammation-mediated status epilepticus
human disease
acute endophthalmitis
Human disease
Acute eosinophilic pneumonia
medical condition
acute erythroid leukemia
rare form of acute myeloid leukemia (less than 5% of AML cases) where the myeloproliferation is of erythroblastic precursors.
ICD: C94.0MeSH: D004915
acute fatty liver of pregnancy
medical condition
ICD: O26.6MeSH: C537957
acute generalized exanthematous pustulosis
widespread acute rash characterized by fever and multiple small pustules on a reddish background
MeSH: D056150
acute graft versus host disease
syndrome of immunologically mediated tissue damage that may occur following an allogeneic transplant, usually affecting the skin, liver, and GI tract. The onset is usually within one hundred days of transplantation or immunologic manipulation
acute hepatic porphyria
acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
human disease
acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome
autosomal recessive cerebellar ataxia that has material basis in homozygous or compound heterozygous mutation in the SCYL1 gene on chromosome 11q13
acute infantile liver failure-multisystemic involvement syndrome
human disease
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