Disease Index
9,486 diseasesother inborn metabolic disease
human disease
other metabolic disease with epilepsy
human disease
other metabolic disease with skin involvement
human disease
other rare diabetes mellitus
human disease
other syndrome with a central nervous system malformation as major feature
human disease
Otodental syndrome
congenital disorder of digestive system
MeSH: C563482
otofaciocervical syndrome
medical condition
otofaciocervical syndrome 1
human disease
otomandibular dysplasia
human disease
otomandibular dysplasia associated with monogenic syndromes
human disease
Otoonychoperoneal syndrome
human disease
MeSH: C564912
otopalatodigital syndrome
x-linked recessive genetic disorders
otopalatodigital syndrome spectrum disorder
otopalatodigital syndrome type 1
ICD: Q87.0
otopalatodigital syndrome type 2
MeSH: C538089
otosclerosis
otitis interna characterized by an abnormal bone growth in the middle ear
MeSH: D010040
otosclerosis 5
human disease
otospondylomegaepiphyseal dysplasia
osteochondrodysplasia that results from mutations in the COL11A2 gene which results in enlargement of the located in epiphysis in located in hand and located in foot, distinct facial features, platyspondyly and hearing loss
ICD: Q77.7
otospondylomegaepiphyseal dysplasia, autosomal dominant
human disease
otulipenia
Human disease
ovarian benign neoplasm
human disease
ICD: D27
ovarian cancer
female reproductive organ cancer that is located in the ovary
ovarian carcinosarcoma
Human disease
ovarian clear cell adenocarcinoma
Human disease
Ovarian fibroma
benign neoplasm arising from soft tissue of the ovary. It is characterized by the presence of spindle-shaped fibroblasts
MeSH: C562391
ovarian fibrothecoma
10cm) are often associated with pleural effusion and ascytes (the Meig's syndrome triad)
ovarian gynandroblastoma
ovarian hyperstimulation syndrome
human disease
ICD: N98.1MeSH: D016471
ovarian mucinous adenocarcinoma
human disease
ovarian small cell carcinoma
Human disease