Disease Index
9,486 diseasesherpes gestationis
dermatosis of pregnancy
MeSH: D006559
herpes simplex virus keratitis
keratitis of the cornea that has material basis in herpes simplex type infection
ICD: B00.5MeSH: D016849
Herpes simplex virus meningoencephalitis
Human disease
MeSH: D020803
Hexokinase deficiency
medical condition
ICD: D55.2MeSH: C562995
hidrotic ectodermal dysplasia, Christianson-Fourie type
human disease
MeSH: C536180
hidrotic ectodermal dysplasia, Halal type
MeSH: C535621
high altitude pulmonary edema
human disease
ICD: T70.2MeSH: C535833
high anorectal malformation
high bone mass osteogenesis imperfecta
human disease
high grade astrocytic tumor
anaplastic astrocytoma (grade III astrocytic tumor) or glioblastoma (grade IV astrocytic tumor)
high grade B-cell lymphoma with MYC and/or BCL2 and/or BCL6 rearrangement
human disease
high myopia-sensorineural deafness syndrome
high-grade neuroendocrine carcinoma of the cervix uteri
human disease
high-grade neuroendocrine carcinoma of the corpus uteri
human disease
Hinman syndrome
Hinman syndrome (HS) or non-neurogenic neurogenic bladder is a voiding dysfunction of the bladder of neuropsychological origin that is characterized by functional bladder outlet obstruction in the absence of neurologic deficits
ICD: N32.8
hip dysplasia, Beukes type
human disease
ICD: Q65.8MeSH: C564185
Hirata disease
autoimmune disease of endocrine system characterized by hypoglycemia caused by antibodies to insulin
Hirschsprung disease-deafness-polydactyly syndrome
medical condition
Hirschsprung disease-ganglioneuroblastoma syndrome
human disease
MeSH: C538119
Hirschsprung disease-nail hypoplasia-dysmorphism syndrome
medical condition
MeSH: C535615
Hirschsprung disease-type D brachydactyly syndrome
medical condition
MeSH: C538319
Hirschsprung's disease
congenital disorder of digestive system
MeSH: D006627
Hirsutism-skeletal dysplasia-intellectual disability syndrome
human disease
MeSH: C536705
histidine metabolism disease
amino acid metabolic disorder that involves deficiency in histidine
histidinemia
histidine metabolism disease that involves a deficiency of the enzyme histidase
ICD: E70.8MeSH: C538320
histidinuria due to a renal tubular defect
human disease
MeSH: C538321
histiocytic and dendritic cell cancer
sarcoma and hematologic cancer that derives from follicular lymphoma
histiocytic sarcoma
medical condition
MeSH: D054747
histoplasmosis
human disease
ICD: B3939.MeSH: D006660
HIV wasting syndrome
Human disease
MeSH: D019247