All Diseases

Showing 7,901–8,000 of 16,077 diseases

Immunodeficiency 87 and autoimmunity

Immunodeficiency 88

Immunodeficiency 91 and hyperinflammation

Immunodeficiency 92

Immunodeficiency 93 and hypertrophic cardiomyopathy

Immunodeficiency 96

Immunodeficiency 97 with autoinflammation

Immunodeficiency 98 with autoinflammation, X-linked

Immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias

Immunodeficiency disease

Immunodeficiency due to a late component of complement deficiency

Immunodeficiency due to MASP-2 deficiency

Immunodeficiency due to selective anti-polysaccharide antibody deficiency

Immunodeficiency-centromeric instability-facial anomalies syndrome

Immunodeficiency-centromeric instability-facial anomalies syndrome 1

Immunodeficiency-centromeric instability-facial anomalies syndrome 2

Immunodeficiency-centromeric instability-facial anomalies syndrome 3

Immunodeficiency-centromeric instability-facial anomalies syndrome 4

Immunodeficiency-related disorder

Immunodeficiency, common variable, 10

Immunodeficiency, common variable, 12

Immunodeficiency, common variable, 5

Immunodeficiency, common variable, 6

Immunodeficiency, common variable, due to APRIL deficiency

Immunoglobulin A deficiency 2

Immunoglobulin A vasculitis

Immunoglobulin G4-related sclerosing disease

Immunoglobulin heavy-and-light chain

Immunoglobulin-mediated membranoproliferative glomerulonephritis

Immunoproliferative disorder

Immunotactoid glomerulopathy

Immunotactoid or fibrillary glomerulopathy

Immunotherapy induced hypophysitis

Impaired renal function disease

IMPDH1-related retinopathy

Imperforate anus

Imperforate oropharynx-costo vetebral anomalies syndrome

Impetigo

Impetigo herpetiformis

IMPG1-related dominant retinopathy

IMPG1-related recessive retinopathy

IMPG2-related dominant retinopathy

IMPG2-related recessive retinopathy

Impulse control disorder

In situ carcinoma

Inappropriate ADH syndrome

Inborn aminoacylase deficiency

Inborn carbohydrate metabolic disorder

Inborn disorder of amino acid metabolism

Inborn disorder of aspartate family metabolism

Inborn disorder of bile acid synthesis

Inborn disorder of bilirubin metabolism

Inborn disorder of branched-chain amino acid metabolism

Inborn disorder of cobalamin metabolism and transport

Inborn disorder of energy metabolism

Inborn disorder of glutamate/glutamine and aspartate/asparagine metabolism

Inborn disorder of glycine and serine metabolism

Inborn disorder of histidine metabolism

Inborn disorder of ketolysis

Inborn disorder of lysine, hydroxylysine, and tryptophan metabolism

Inborn disorder of methionine cycle and sulfur amino acid metabolism

Inborn disorder of ornithine metabolism

Inborn disorder of ornithine, proline and hydroxyproline metabolism

Inborn disorder of porphyrin metabolism

Inborn disorder of proline metabolism

Inborn disorder of purine metabolism

Inborn disorder of pyridoxine metabolism

Inborn disorder of pyrimidine metabolism

Inborn disorder of serine family metabolism

Inborn disorder of the metabolism of sulfur-containing amino acids and hydrogen sulfide

Inborn disorder of tryptophan metabolism

Inborn error of immunity

Inborn errors of metabolism

Inborn glycerol kinase deficiency

Inborn metal metabolism disorder

Inborn mitochondrial metabolism disorder

Inborn mitochondrial myopathy

Inborn organic aciduria

Inborn serine deficiency

Inborn vitamin metabolic disorder

Incessant infant ventricular tachycardia

Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2

Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3

Inclusion body myopathy with Paget disease of bone and frontotemporal dementia

Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1

Inclusion body myositis

Inclusion conjunctivitis

Incomplete septal cirrhosis

Incontinentia pigmenti

Indeterminate colitis

Indeterminate dendritic cell tumor

Indeterminate leprosy

Indian tick typhus

Indolent systemic mastocytosis

Indomethacin embryofetopathy

Infant botulism

Infant epilepsy with migrant focal crisis

Infant gynecomastia

Infant-type hemispheric glioma

Infantile apnea

Showing 7,901–8,000 of 16,077 diseases