Disease Index
9,486 diseasesanorchia
condition where one is born without testes
ICD: Q55.0|
anorectal anomalies
human disease
MeSH: C537771
ANOTHER syndrome
human disease
MeSH: C565604
Anotia
medical condition
ICD: Q17.0MeSH: C537772
antecubital pterygium syndrome
human disease
MeSH: C566738
antenatal multiminicore disease with arthrogryposis multiplex congenita
human disease
anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis
human disease
MeSH: C537694
anterior segment dysgenesis 7
human disease
anterior segment mesenchymal dysgenesis
Human disease
anterior urethral valve
human disease
anterior uveitis
Human disease
MeSH: D014606
Anti-HLA hyperimmunization
Anti-HLA hyperimmunization is an increase in anti-HLA antigens mostly seen in chronic renal failure (CRF) patients that have undergone hemodialysis and polytransfusion
Anti-IgLON5 disease
human disease
anti-Kell hemolytic disease of the newborn
human disease
ICD: P55.8
Anti-MAG peripheral neuropathy
Polyneuropathy associated with IgM monoclonal gammapathy (MG) with anti-MAG (myelin-associated-glycoprotein) activity is a demyelinating polyneuropathy characterized clinically by sensory ataxia, tremor, paresthesia, and impaired gait
anti-neutrophil cytoplasmic antibody-associated vasculitis
group of systemic vasculitis conditions with a strong association with ANCA
MeSH: D056648
anti-p200 pemphigoid
human disease
antisynthetase syndrome
human disease
MeSH: C537778
antithrombin III deficiency
inherited blood coagulation disease characterized by the tendency to form clots in the veins
MeSH: D020152
Antley-Bixler syndrome
autosomal recessive disease that is characterized at birth or prenatally by malformations and deformities affecting the majority of the skeleton and other areas of the body with autosomal recessive inheritance of the FGFR2 gene
ICD: Q87.0MeSH: D054882
Antley-Bixler syndrome with genital anomalies and Disordered steroidogenesis
human disease
aortic arch anomaly-facial dysmorphism-intellectual disability syndrome
medical condition
MeSH: C537785
aortic arch defects
human disease
aortic malformation
human disease
aortic valve atresia
rare congenital heart defect characterized by the complete failure of the aortic valve to open. It is manifested during infancy with cyanosis, dyspnea, and rapidly progressing heart failure
aortic valve dysplasia
human disease
aorto-left ventricular tunnel
human disease
aorto-right ventricular tunnel
human disease
aorto-ventricular tunnel
Aorto-ventricular tunnel is a congenital, extracardiac channel which connects the ascending aorta above the sinotubular junction to the cavity of the left, or (less commonly) right ventricle
aortopulmonary coronary arterial course
human disease