Disease Index
9,486 diseasespili torti-developmental delay-neurological abnormalities syndrome
MeSH: C537398
pili torti-onychodysplasia syndrome
Pili torti-onychodysplasia is a form of ectodermal dysplasia characterised by dystrophy of the distal part of the nails and trichodysplasia. It has been described in only one family. Transmission is autosomal recessive.
MeSH: C537399
pilocytic astrocytoma
astrocytoma that is characterized by cells that look like fibers when viewed under a microscope and is located in the brain
ICD: C71
Pilodental dysplasia-refractive errors syndrome
human disease
MeSH: C535763
pilomatrixoma
Human disease
ICD: D23MeSH: D018296
pilomyxoid astrocytoma
Human disease
Pilotto syndrome
human disease
MeSH: C537400
pineal parenchymal tumor of intermediate differenciation
pineal tumor of neuroepithelial tissue
human disease
pinealoblastoma
pineal gland neoplasm located in the brain
ICD: C75.3
Pineocytoma
medical condition
Pipecolic acidemia
a very rare autosomal recessive metabolic disorder that is caused by a peroxisomal defect
Pitt-Hopkins syndrome
rare genetic disorder characterized by developmental delay, epilepsy, distinctive facial features, and possible intermittent hyperventilation followed by apnea
MeSH: C537403
Pitt-Hopkins-like syndrome
human disease
Pitt–Rogers–Danks syndrome
Pituicytoma
medical condition
ICD: C75.1
pituitary adenoma
Human disease
ICD: D35.2
pituitary apoplexy
Human disease
ICD: E23.6MeSH: D010899
pituitary cancer
endocrine gland cancer located in the pituitary gland located at the base of the brain
pituitary carcinoma
human disease
pituitary deficiency
human disease
pituitary deficiency due to empty sella turcica syndrome
human disease
pituitary deficiency due to Rathke's pouch cysts
human disease
pituitary dermoid and epidermoid cysts
human disease
pituitary hormone deficiency from meningeal origin
human disease
pituitary hormone deficiency from tumoral origin
human disease
pituitary hormone deficiency secondary to a granulomatous disease
human disease
pituitary hormone deficiency secondary to storage disease
human disease
pituitary hormone defiency from vascular origin
human disease
pityriasis rubra pilaris
Human disease
MeSH: D010916