Rare Disease Index
9,491 diseasesPrader-Willi syndrome due to point mutation
human disease
Prader-Willi syndrome due to translocation
human disease
Prader-Willi-like syndrome
human disease
Prader-Willi-like syndrome due to point mutation
human disease
Prader–Willi syndrome
rare genetic disorder
MeSH: D011218
Prata-Liberal-Goncalves syndrome
human disease
MeSH: C538180
Pre-Descemet corneal dystrophy
Pre-Descemet corneal dystrophy (PDCD) is a rare form of stromal corneal dystrophy characterized by focal, fine, gray opacities in the deep stroma immediately anterior to the Descemet membrane, with no effect on vision
pre-eclampsia
hypertension occurring during pregnancy
MeSH: D011225
preauricular sinus and cyst
human anatomy
ICD: Q18.1
preaxial polydactyly of fingers
preaxial polydactyly of toes
human disease
preaxial polydactyly of toes, bilateral
human disease
preaxial polydactyly of toes, unilateral
human disease
preaxial polydactyly-colobomata-intellectual disability syndrome
MeSH: C537888
precancerous lesion of palpebral epidermis
precancerous condition that involves the skin of eyelid
precocious puberty
human disease
ICD: E22.8MeSH: D011629
precocious puberty in female
human disease
precursor B-cell acute lymphoblastic leukemia
human disease
ICD: C83.5
precursor T-cell acute lymphoblastic leukemia
human disease
precursor T-cell lymphoblastic leukemia
human disease
MeSH: D054218
predominantly large-vessel vasculitis
human disease
predominantly medium-vessel vasculitis
human disease
prelingual non-syndromic genetic deafness
human disease
premature closure of the arterial duct
human disease
premature ovarian failure
ovarian disease where ovaries do not produce estrogen despite high levels of circulating gonadotropins in women under 40
MeSH: D016649
Prenatal benign hypophosphatasia
prenatal cocaine exposure
exposure of a fetus to cocaine when a pregnant woman uses the drug
prenatal-onset spinal muscular atrophy with congenital bone fractures
human disease
presynaptic congenital myasthenic syndrome
human disease
pretibial dystrophic epidermolysis bullosa
Pretibial dystrophic epidermolysis bullosa is a rare subtype of dystrophic epidermolysis bullosa (DEB, see this term) characterized by the development of blisters, erosions, and lichenoid lesions predominantly in the pretibial region
MeSH: C535494