Disease Index
9,486 diseasesavian influenza
influenza caused by viruses adapted to birds
ICD: J09.009.0MeSH: D005585
Axenfeld anomaly
Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities
human disease
MeSH: C566234
Axenfeld-Rieger syndrome
autosomal dominant disease characterized by abnormalities of the front part of the eye, the anterior segment
MeSH: C535679
axial mesodermal dysplasia spectrum
human disease
MeSH: C537790
axial spondylometaphyseal dysplasia
MeSH: C535795
AXIN2-related attenuated familial adenomatous polyposis
human disease
axonal hereditary motor and sensory neuropathy
human disease
axonal polyneuropathy associated with IgG/IgM/IgA monoclonal gammopathy
human disease
Ayazi syndrome
medical condition
MeSH: C537793
Ayme-Gripp syndrome
human disease
MeSH: C563390
Azoor
disease
ICD: H35.0MeSH: C538223
azoospermia
male infertility disease characterized by the absence of any measurable level of sperm in semen
MeSH: D053713
Azygos continuation
human disease
B-cell non-Hodgkin lymphoma
The most common type of non-Hodgkin lymphoma. It includes the most frequently seen morphologic variants which are: diffuse large B-cell lymphoma, follicular lymphoma, small lymphocytic lymphoma and marginal zone B-cell lymphoma. -- 2003
B-cell prolymphocytic leukemia
neoplasm of prolymphocytes affecting the blood, bone marrow, and spleen.
MeSH: D054403
Babesiosis
malaria-like parasitic disease caused by infection with Babesia and nalga, a genus of Apicomplexa
MeSH: D001404
bacterial infectious disease
disease caused by bacteria
ICD: A49.9MeSH: D001424
bacterial myositis
human disease
Bainbridge Ropers Syndrome
Human genetic disorder
Bálint's syndrome
uncommon and incompletely understood triad of severe neuropsychological impairments
Ballard syndrome
brachydactyly characterized by autosomal dominant inheritance of hypoplasia of the distal phalanges of the ulnar side of the hand and shortening of one or more metacarpals but normal stature
MeSH: C537094
Baller-Gerold syndrome
synostosis characterized by coronal craniosynostosis, short stature, and aplasia or hypoplasia of the radial bone
MeSH: C536788
Balo concentric sclerosis
demyelinating disease characterized by the fact that the demyelinated tissues form concentric layers
Bamforth-Lazarus syndrome
Human disease
MeSH: C537901
Bangstad syndrome
medical condition
MeSH: C537902
Banki syndrome
medical condition
MeSH: C566228
Bannayan-Riley-Ruvalcaba syndrome
a rare overgrowth syndrome and hamartomatous disorder with occurrence of multiple subcutaneous lipomas, macrocephaly and hemangiomas.
BAP1-related tumor predisposition syndrome
human disease
Baraitser-Winter syndrome
Human disease