Disease Index
9,486 diseaseshuman herpesvirus 8 infectious disease
Human disease
human infection by orthopoxvirus
human disease
humeral agenesis/hypoplasia
humeral agenesis/hypoplasia, bilateral
human disease
humeral agenesis/hypoplasia, unilateral
human disease
Humero-radial synostosis, bilateral
human disease
Humero-radial synostosis, unilateral
human disease
Humero-radio-ulnar synostosis
human disease
Humero-radio-ulnar synostosis, bilateral
human disease
Humero-radio-ulnar synostosis, unilateral
human disease
humero-ulnar synostosis
human disease
Humero-ulnar synostosis, bilateral
human disease
Humero-ulnar synostosis, unilateral
human disease
humeroradial synostosis
Human disease
MeSH: C535284
humerus trochlea aplasia
MeSH: C566022
Hunter-Macdonald syndrome
human disease
MeSH: C567445
Hunter-McAlpine craniosynostosis
MeSH: C536072
Huntington disease-like 1
human disease
MeSH: C566398
Huntington disease-like 2
Huntington disease-like 2 (HDL2) is a severe neurodegenerative disorder considered part of the neuroacanthocytosis syndromes (see this term) characterized by a triad of movement, psychiatric, and cognitive abnormalities
MeSH: C564708
Huntington disease-like 3
human disease
MeSH: C565747
Huntington disease-like syndrome due to C9ORF72 expansions
human disease
Huntington's disease
rare neurodegenerative disorder of the central nervous system characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia
ICD: F02.2MeSH: D006816
Huntington's disease-like syndrome
human disease
MeSH: C580174
HUPRA syndrome
human disease
Hurler syndrome
genetic disorder that results in the buildup of glycosaminoglycans (AKA GAGs, or mucopolysaccharides) due to a deficiency of alpha-L iduronidase
Hurler–Scheie syndrome
MPS - I H/S: cutaneous condition, also characterized by mild mental retardation and corneal clouding
hyaline body myopathy
human disease
hydranencephaly
congenital disorder of nervous system
MeSH: D006832
hydranencephaly with renal aplasia-dysplasia
human disease
MeSH: C565507
hydroa vacciniforme
rare skin disorder of unknown etiology affecting children
ICD: L56.8MeSH: D006837