Disease Index
9,486 diseasesprogressive demyelinating neuropathy with bilateral striatal necrosis
human disease
progressive encephalomyelitis with rigidity and myoclonus
human disease
progressive epilepsy and/or ataxia with myoclonus as a major feature
human disease
progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome
human disease
progressive familial heart block
human disease
progressive familial intrahepatic cholestasis
intrahepatic cholestasis characterized by early onset of chronic unremitting cholestasis of hepatocellular origin that progresses to hepatic fibrosis, cirrhosis, and end-stage liver disease before adulthood
progressive familial intrahepatic cholestasis 1
progressive familial intrahepatic cholestasis characterized by autosomal recessive inheritance that has material basis in mutation in the ATP8B1 gene on chromosome 18q21
MeSH: C535933
progressive familial intrahepatic cholestasis 2
progressive familial intrahepatic cholestasis characterized by autosomal recessive inheritance that has material basis in mutation in the ABCB11 gene on chromosome 2q31
MeSH: C535934
progressive familial intrahepatic cholestasis 3
progressive familial intrahepatic cholestasis characterized by autosomal recessive inheritance of intrahepatic cholestasis and elevated serum GGT1 activity that has material basis in mutation in the ABCB4 gene on chromosome 7q21.12
MeSH: C535935
progressive familial intrahepatic cholestasis 5
human disease
progressive familial intrahepatic cholestasis type 4
human disease
progressive iris atrophy
Human disease
ICD: H21.2
progressive microcephaly-seizures-cortical blindness-developmental delay syndrome
human disease
progressive multifocal leukoencephalopathy
viral disease affecting human brains
MeSH: D007968
progressive muscular atrophy
rare, milder form of amyotrophic lateral sclerosis. It is characterized by a slowly progressive clinical course. Signs and symptoms include muscle weakness, atrophy, and fasciculation
progressive muscular dystrophy
human disease
progressive myoclonic epilepsy type 3
human disease
progressive myoclonic epilepsy type 5
human disease
progressive myoclonic epilepsy type 7
human disease
progressive myoclonic epilepsy type 8
human disease
progressive myoclonic epilepsy type 9
human disease
progressive myoclonic epilepsy with dystonia
progressive myoclonus epilepsy
Human disease
MeSH: D020191
Progressive nodular histiocytosis
medical condition
progressive nonfluent aphasia
neurological disorder
MeSH: D057178
progressive osseous heteroplasia
gene (20q13.2-q13.3), coding for guanine nucleotide-binding proteins. POH can, however, be distinguished clinically by the deep and progressive nature of the heterotopic bone formation.
MeSH: C562735
progressive pseudorheumatoid arthropathy of childhood
Progressive pseudorheumatoid arthropathy (dysplasia) of childhood (PPAC; PPD) presents as spondyloepiphyseal dysplasia (SED) tarda with progressive arthropathy and is described as a specific autosomal recessive subtype of SED
MeSH: C535387
progressive retinal dystrophy due to retinol transport defect
human disease
progressive rubella panencephalitis
human disease
progressive scapulohumeroperoneal distal myopathy
human disease