Disease Index
9,486 diseasesaniridia
Human disease
MeSH: D015783
aniridia ataxia renal agenesis psychomotor retardation
medical condition
MeSH: C000598722
aniridia-absent patella syndrome
MeSH: C566281
aniridia-intellectual disability syndrome
MeSH: C536568
aniridia-ptosis-intellectual disability-familial obesity syndrome
anisakiasis
helminthiasis
MeSH: D017129
ankyloblepharon filiforme adnatum-cleft palate syndrome
human disease
MeSH: C536373
ankyloblepharon filiforme-imperforate anus syndrome
human disease
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
human disease
MeSH: C535289
ankylosing spondylitis
type of arthritis in which there is long term inflammation of the joints of the spine
MeSH: D013167
Ankylosing vertebral hyperostosis with tylosis
medical condition
annular atrophic lichen planus
Annular atrophic lichen planus (LP) is a rare variant of cutaneous lichen planus (see this term) characterized by both annular and atrophic LP (see these terms) features in the same lesion
annular epidermolytic ichthyosis
MeSH: C564367
Annular lichen planus
Annular lichen planus (LP) is a rare variant of cutaneous lichen planus (see this term) characterized by the development of annular lesions
ICD: L43.8
annular pancreas
pancreas disease characterized by autosomal dominant inheritance of the annular pancreas (head of the pancreas forming a ring around the second portion of the duodenum) and duodenal stenosis
MeSH: C536376
anodontia
human disease
MeSH: D000848
anomaly of puberty or/and menstrual cycle
human disease
anomaly of puberty or/and menstrual cycle of genetic origin
instance of anomaly of puberty or/and menstrual cycle that is caused by a modification of the individual's genome
anomaly of the mitral subvalvular apparatus
human disease
anomaly of the secretory and excretory apparatus of the lacrimal system
human disease
anomaly of the tricuspid subvalvular apparatus
human disease
anomaly of the tricuspid valve chordae
human disease
anonychia congenita
Human disease
ICD: Q84.3MeSH: C536377
anonychia with flexural pigmentation
human disease
MeSH: C566278
anonychia-microcephaly syndrome
MeSH: C536948
anonychia-onychodystrophy syndrome
human disease
MeSH: C536378
anonychia-onychodystrophy with brachydactyly type b and ectrodactyly
human disease
MeSH: C536379
anophthalmia plus syndrome
MeSH: C537767
anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome
human disease
anophthalmia-microphthalmia syndrome
human disease