Disease Index
9,486 diseasesimmunodeficiency syndrome with abnormal pigmentation
human disease
immunodeficiency syndrome with autoimmunity
human disease
immunodeficiency with factor H anomaly
human disease
immunodeficiency with isotype or light chain deficiencies with normal number of B-cells
human disease
immunodeficiency with severe reduction in serum IgG and IgA with normal/elevated IgM and normal number of B-cells
human disease
immunodeficiency-associated lymphoproliferative disease
human disease
immunodeficiency-centromeric instability-facial anomalies syndrome
autosomal recessive disease characterized by immunodeficiency, rearrangements in the vicinity of the centromeres of chromosomes 1, 9, and 16 and facial anomalies in most cases
immunodeficiency-centromeric instability-facial anomalies syndrome 1
human disease
MeSH: C537362
immunoglobulin A deficiency
dysgammaglobulinemia characterized by a deficiency of immunoglobulin A
MeSH: D017098
immunoglobulin A deficiency 1
human disease
MeSH: C536290
immunoglobulin A deficiency 2
human disease
MeSH: C536291
immunoglobulin heavy chain deficiency
human disease
immunoglobulin-mediated membranoproliferative glomerulonephritis
human disease
immunotactoid glomerulopathy
kidney disease
Immunotactoid or fibrillary glomerulopathy
imperforate oropharynx-costo vetebral anomalies syndrome
human disease
impossible syndrome
complex combination of human congenital malformations (birth defects)
inborn aminoacylase deficiency
acquired metabolic disease that is has its basis in the disruption of aminoacylase activity
inborn disorder of bilirubin metabolism
instance of bilirubin metabolism disease that is caused by an inherited modification of the individual's genome
inborn disorder of branched-chain amino acid metabolism
acquired metabolic disease that is has its basis in the disruption of branched-chain amino acid metabolic process
inborn disorder of cobalamin metabolism and transport
human disease
inborn disorder of energy metabolism
acquired metabolic disease that is has its basis in the disruption of generation of precursor metabolites and energy
inborn disorder of fatty acid oxidation and ketone body metabolism
human disease
inborn disorder of gamma-aminobutyric acid metabolism
acquired metabolic disease that is has its basis in the disruption of gamma-aminobutyric acid metabolic process
inborn disorder of glycerol metabolism
acquired metabolic disease that is has its basis in the disruption of glycerol metabolic process
inborn disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation
human disease
inborn disorder of ketolysis
acquired metabolic disease that is has its basis in the disruption of ketone body catabolic process
inborn disorder of lysosomal amino acid transport
human disease
inborn disorder of neurotransmitter metabolism and transport
human disease
inborn disorder of ornithine or proline metabolism
human disease