Disease Index
9,486 diseasespolydactyly of a triphalangeal thumb, bilateral
human disease
polydactyly of a triphalangeal thumb, unilateral
human disease
polydactyly of an index finger
MeSH: C566784
polydactyly of an index finger, bilateral
human disease
polydactyly of an index finger, unilateral
human disease
polydactyly-myopia syndrome
medical condition
MeSH: C536331
polyembryoma
medical condition
polyendocrine-polyneuropathy syndrome
human disease
polyglandular dysfunction
human disease
ICD: E31
polyglucosan body myopathy 1 with or without immunodeficiency
human disease
polyglucosan body myopathy type 2
human disease
polymalformative genetic syndrome with increased risk of developing cancer
Polymalformative genetic syndrome with increased risk of developing cancer (PGSIRC) comprises a wide range of syndromes characterized by congenital malformations with a high risk of developing tumors including up to 50 different rare diseases
Polymerase proofreading-related adenomatous polyposis
human disease
polymicrogyria
condition that affects the development of the human brain by multiple small gyri (microgyri) creating excessive folding of the brain leading to an abnormally thick cortex
MeSH: D065706
polymicrogyria with optic nerve hypoplasia
human disease
MeSH: C567715
polymicrogyria-turricephaly-hypogenitalism syndrome
human disease
polymyalgia rheumatica
syndrome with pain or stiffness, usually in the neck, shoulders, upper arms, and hips, but which may occur all over the body
MeSH: D011111
polymyositis
rare idiopathic inflammatory myopathy characterized by symmetric proximal muscle weakness and elevated muscle enzymes
ICD: M33.2MeSH: D017285
polyneuropathy-hand defect syndrome
human disease
MeSH: C535624
Polyneuropathy-intellectual disability-acromicria-premature menopause syndrome
rare disease
polyostotic fibrous dysplasia
autosomal dominant disease that involves skin pigmentation, bone and hormonal problems along with premature puberty
MeSH: D005359
Polyostotic osteolytic dysplasia, hereditary expansile
human disease
MeSH: C536335
polyploidy
chromosomal constitution of a cell containing multiples of the normal number of chromosomes
MeSH: D011123
polyradiculoneuropathy associated with IgG/IgA/IgM monoclonal gammopathy without known antibodies
human disease
polyrrhinia
polysomy of X chromosome
human disease
ICD: Q97
polysyndactyly
medical condition
ICD: Q70.4
polysyndactyly-cardiac malformation syndrome
facial dysmorphism, hepatic cysts)
MeSH: C564875
polysyndactyly, bilateral
human disease
polysyndactyly, unilateral
human disease