Disease Index
9,486 diseasesundifferentiated connective tissue disease
autoimmune disorder which does not meet classification criteria used to establish the presence of other well-defined connective tissue diseases
MeSH: D000074079
undifferentiated embryonal sarcoma of the liver
undifferentiated juvenile idiopathic arthritis
human disease
undifferentiated pleomorphic sarcoma
medical condition
ICD: C49MeSH: D051677
unexplained long-lasting fever/inflammatory syndrome
human disease
unexplained periodic fever syndrome
human disease
unicameral bone cyst
solitary bone cyst is a benign non-epithelial bone cavity that is asymptomatic and that is found most commonly in the second decade of life by chance. The long bones are most often affected, but cases involving the jaw bone have been reported
Unicentric Castleman disease
Localized Castleman disease (LCD) is the most common form of Castleman disease (CD; see this term) and it is usually asymptomatic or it may present with enlarged lymph nodes. LCD may be cured by surgical resection.
unicervical bicornuate uterus
human disease
unilateral aplasia of the mullerian ducts
human disease
unilateral congenital megacalycosis
human disease
unilateral focal polymicrogyria
unilateral hemispheric polymicrogyria
human disease
unilateral polymicrogyria
uniparental disomy 14
Uniparental disomy of chromosome 11
UPD(11)
MeSH: C536468
uniparental disomy of chromosome X
human disease
uniparental disomy of maternal origin
human disease
uniparental disomy of paternal origin
human disease
univentricular cardiopathy
human disease
univentricular heart
ICD: Q20.4MeSH: D000080039
univentricular heart with single atrio-ventricular valve
Orphanet summary for this disease is currently under development. However, other data related to the disease are accessible from the Additional Information menu located on the right side of this page
unknown leukodystrophy
human disease
Unna–Thost disease
ICD: Q82.8
unspecified mitochondrial disorder
human disease
unstable hemoglobin disease
human disease
Unverricht-Lundborg syndrome
Human disease
ICD: G40.3MeSH: D020194
Upington disease
medical condition
ICD: M91.8MeSH: C536472
upper limb defect-eye and ear abnormalities syndrome
MeSH: C564769
upper limb hypertrophy
human disease