Disease Index

9,486 diseases
Harding ataxia
medical condition
MeSH: C535633
Harel-Yoon syndrome
human disease
harlequin syndrome
condition characterized by asymmetric sweating and flushing on the upper thoracic region of the chest, neck and face
MeSH: C535634
Harrod syndrome
MeSH: C535635
Hartnup disease
Human disease
MeSH: D006250
Hartsfield-Bixler-Demyer syndrome
human disease
MeSH: C564484
Hashimoto's encephalopathy
human disease
MeSH: C535841
Haverhill fever
Human disease
hawkinsinuria
disease
ICD: E72.1MeSH: C535845
HCL-V
Human disease
head and neck cancer
organ system cancer in the head or neck region
ICD: C07
head and neck squamous cell carcinoma
head and neck carcinoma that has material basis in squamous cells that line the moist, mucosal surfaces inside the head and neck
MeSH: D000077195
hearing loss-familial salivary gland insensitivity to aldosterone syndrome
heart arrhythmia
group of conditions in which the heartbeat is irregular, too fast, or too slow
ICD: I47MeSH: D001145
heart defect-tongue hamartoma-polysyndactyly syndrome
human disease
MeSH: C535849
heart defects-limb shortening syndrome
MeSH: C535850
heart position anomaly
human disease
Heart valve dysplasia
human disease
MeSH: C535576
heart-hand syndrome type 3
medical condition
MeSH: C535853
heart-hand syndrome, Slovenian type
medical condition
MeSH: C535852
heavy chain deposition disease
human disease
heavy chain disease
hypersensitivity reaction type IV disease that results from a proliferation of cells producing immunoglobulin heavy chains
ICD: C88.2MeSH: D006362
HEC syndrome
medical condition
MeSH: C535855
Hecht-Scott syndrome
human disease
MeSH: C535856
Heimler syndrome 1
human disease
Heiner syndrome
Heinz body anemia
human disease
MeSH: C563030
helicoid peripapillary chorioretinal degeneration
eye disease characterized by presence in the fundus of progressive bilateral retinal and choroidal atrophy leading to central vision loss that has material basis in heterozygous muation in TEAD1 on 11p15.3
MeSH: C566236
HELLP syndrome
severe pre-eclampsia characterized by hemolysis, elevated liver enzyme and low platelet count
ICD: O14.2MeSH: D017359
Helsmoortel-Van Der Aa syndrome
autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of ADNP on chromosome 20q13.13
Page 132 of 317 (9,486 total)