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Disease	Synonyms	Description	Articles
phalanx chondroma		A bone benign neoplasm that is located_in the phal..[+] A bone benign neoplasm that is located_in the phalanx that has_material_basis_in cartilaginous cells. [-]
parietal lobe ependymoma		A parietal lobe neoplasm that has_material_basis_i..[+] A parietal lobe neoplasm that has_material_basis_in cells lining the ventricles of the brain. [-]
pharynx squamous cell carcinoma		A pharynx cancer that has_material_basis_in squamo..[+] A pharynx cancer that has_material_basis_in squamous cells. [-]
parotid gland adenoid cystic carcinoma		A parotid gland cancer that is characterized by a ..[+] A parotid gland cancer that is characterized by a distinctive pattern in which abnormal nests or cords of epithelial cells surround and/or infiltrate ducts or glandular structures within the affected organ. [-]
pervasive developmental disorder	Pervasive Child Development Disorders; pervasive d.. [+] Pervasive Child Development Disorders; pervasive development disorder [-]	A developmental disorder of mental health that ref..[+] A developmental disorder of mental health that refers to a group of five disorders characterized by impairments in socialization and communication, as well as restricted interests and repetitive behaviors. [-]	34 articles
paraphilia disorder		A sexual disorder that is characterized recurrent,..[+] A sexual disorder that is characterized recurrent, intense sexually arousing fantasies, sexual urges or behaviors generally involving nonhuman objects. [-]
popliteal pterygium syndrome	popliteal web syndrome; facio-genito-popliteal syn.. [+] popliteal web syndrome; facio-genito-popliteal syndrome [-]	A syndrome characterized by abnormal development o..[+] A syndrome characterized by abnormal development of the face, skin and genitals. Clinical expressions of the disease include cleft lip, with or without cleft palate, contractures of the lower extremities, abnormal external genitalia, syndactyly of fingers and/or toes, and a pyramidal skin fold over the hallux nail. It has_material_basis_in mutations in the IRF6 gene on chromosome 1. [-]
pyridoxine-responsive sideroblastic anemia		n_a
Pearson syndrome	Pearson Marrow-Pancreas Syndrome	A mitochondrial metabolism disease that is charact..[+] A mitochondrial metabolism disease that is characterized by sideroblastic anemia and exocrine pancreas dysfunction. [-]
pre-malignant neoplasm		A disease of cellular proliferation that results i..[+] A disease of cellular proliferation that results in abnormal growths in the body, which do not invade or destroy the surrounding tissue but, given enough time, will transform into a cancer. [-]
progesterone-receptor positive breast cancer		n_a
progesterone-receptor negative breast cancer		n_a
peritoneal benign neoplasm		A thoracic benign neoplasm that is located_in the ..[+] A thoracic benign neoplasm that is located_in the serous membrane lining the abdominal cavity or coelom. [-]
pharynx cancer	pharyngeal neoplasm; pharynx neoplasm; pharyngeal .. [+] pharynx neoplasm; pharyngeal neoplasm; pharyngeal cancer [-]	A gastrointestinal system cancer that is located_i..[+] A gastrointestinal system cancer that is located_in the pharynx. [-]
pain agnosia	analgesia	An agnosia that is a loss of the ability to percei..[+] An agnosia that is a loss of the ability to perceive and process pain. [-]	2 articles
phonagnosia		An agnosia that is a loss of the ability to recogn..[+] An agnosia that is a loss of the ability to recognize familiar voices. [-]
pain disorder		A somatoform disorder that involves chronic pain i..[+] A somatoform disorder that involves chronic pain in one or more areas, and is thought to be caused by psychological stress. [-]	9 articles
physical urticaria		An urticaria induced by external physical influenc..[+] An urticaria induced by external physical influences. [-]
ptosis	blepharoptosis; drooping eyelid	An eye disease characterized by the drooping or fa..[+] An eye disease characterized by the drooping or falling of the upper or lower eyelid. [-]
porencephaly		A brain disease that is characterized by encephalo..[+] A brain disease that is characterized by encephalomalacia and cystic brain lesions. [-]
pontocerebellar hypoplasia	PCH	A neurodegenerative disease that is characterized ..[+] A neurodegenerative disease that is characterized by underdevelopment of the pons and cerebellum. [-]
pontocerebellar hypoplasia type 1A		A pontocerebellar hypoplasia that is characterized..[+] A pontocerebellar hypoplasia that is characterized by central and peripheral motor dysfunction, hypotonia, spasticity and failure to thrive, has_material_basis_in homozygous or compound heterozygous mutation in the VRK1 gene. [-]
pontocerebellar hypoplasia type 1B		A severe pontocerebellar hypoplasia that is charac..[+] A severe pontocerebellar hypoplasia that is characterized by hypotonia, progressive microcephaly and developmental delay, has_material_basis_in autosomal recessive inheritance of mutation in the EXOSC3 gene. [-]
pontocerebellar hypoplasia type 2A		A severe pontocerebellar hypoplasia that is charac..[+] A severe pontocerebellar hypoplasia that is characterized by progressive microcephaly, chorea, epilepsy and hyperreflexia, has_material_basis_in autosomal recessive inheritance of mutation in the TSEN54 gene. [-]
pontocerebellar hypoplasia type 2B		A severe pontocerebellar hypoplasia that is charac..[+] A severe pontocerebellar hypoplasia that is characterized by progressive microcephaly, clonus, dysphagia and failure to thrive, has_material_basis_in autosomal recessive inheritance of mutation in the TSEN2 gene. [-]
pontocerebellar hypoplasia type 2C		A severe pontocerebellar hypoplasia that is charac..[+] A severe pontocerebellar hypoplasia that is characterized by progressive microcephaly, extrapyramidal dyskinesia, seizure and failure to thrive, has_material_basis_in autosomal recessive inheritance of mutation in the TSEN34 gene. [-]
pontocerebellar hypoplasia type 2D		A pontocerebellar hypoplasia that is characterized..[+] A pontocerebellar hypoplasia that is characterized by progressive microcephaly, profound intellectual disability, spasticity and seizure, has_material_basis_in autosomal recessive inheritance of mutation in the SEPSECS gene. [-]
pontocerebellar hypoplasia type 2E		A pontocerebellar hypoplasia that is characterized..[+] A pontocerebellar hypoplasia that is characterized by progressive microcephaly, profound intellectual disability, spasticity and seizure, has_material_basis_in autosomal recessive inheritance of mutation in the VPS53 gene. [-]
pontocerebellar hypoplasia type 3		A pontocerebellar hypoplasia that is characterized..[+] A pontocerebellar hypoplasia that is characterized by progressive microcephaly, hypotonia, dysmorphic features, profound intellectual disability and seizure, has_material_basis_in autosomal recessive inheritance of mutation in the PCLO gene. [-]
pontocerebellar hypoplasia type 4		A pontocerebellar hypoplasia that is characterized..[+] A pontocerebellar hypoplasia that is characterized by progressive microcephaly, hypertonia, myoclonus, seizure and early lethality, has_material_basis_in autosomal recessive inheritance of mutation in the TSEN54 gene. [-]
pontocerebellar hypoplasia type 5		A pontocerebellar hypoplasia that is characterized..[+] A pontocerebellar hypoplasia that is characterized by severe olivopontocerebellar hypoplasia and degeneration leading to early lethality, has_material_basis_in autosomal recessive inheritance of mutation in the TSEN54 gene. [-]
pontocerebellar hypoplasia type 6		A pontocerebellar hypoplasia that is characterized..[+] A pontocerebellar hypoplasia that is characterized by olivopontocerebellar hypoplasia and developmental delay, has_material_basis_in autosomal recessive inheritance of mutation in the RARS2 gene. [-]
pontocerebellar hypoplasia type 7		n_a
pontocerebellar hypoplasia type 8		n_a
pontocerebellar hypoplasia type 9		n_a
pontocerebellar hypoplasia type 10		n_a
primary pigmented nodular adrenocortical disease		An adrenal cortex disease characterized by small t..[+] An adrenal cortex disease characterized by small to normal sized adrenal glands containing multiple small cortical pigmented nodules. [-]
photosensitive epilepsy	photoparoxysmal response; photogenic epilepsy	An epilepsy characterized by seizures triggered by..[+] An epilepsy characterized by seizures triggered by visual stimuli that form patterns in space or time, such as flashing lights. [-]
persistent hyperplastic primary vitreous		A developmental vitreous disease that is character..[+] A developmental vitreous disease that is characterized by leukocoria, strabismus and vision loss, caused by failure of primary vitreous and hyaloid vasculature to regress during embryological development. [-]
peeling skin syndrome	peeling skin disease; PSS; deciduous skin; familia.. [+] PSS; peeling skin disease; deciduous skin; familial continuous skin peeling syndrome; keratosis exfoliativa congenita [-]	A skin disease that is characterized by the painle..[+] A skin disease that is characterized by the painless, continuous peeling of the top layer of skin. [-]
paroxysmal nocturnal hemoglobinuria		An acquired hemolytic anemia that is characterized..[+] An acquired hemolytic anemia that is characterized by abdominal pain, hematuria, esophageal dysmotility and thrombosis, has_material_basis_in defect in the cell membrane glycosyl phosphatidylinositols that protect red blood cells from the innate complement immune system. [-]
parietal foramina	Caitlin marks; enlarged parietal foramina; heredit.. [+] Caitlin marks; enlarged parietal foramina; hereditary cranium bifidum [-]	An inherited neural tube defect that is characteri..[+] An inherited neural tube defect that is characterized by enlarged openings in the parietal bones of the skull, has_material_basis_in mutation in the ALX4 gene or MSX2 gene. [-]
persistent generalized lymphadenopathy	PGL	A lymph node disease characterized by enlarged, no..[+] A lymph node disease characterized by enlarged, non-painful lymph nodes occurring for more than three to six months for which no other reason can be found. [-]
parameningeal embryonal rhabdomyosarcoma		An embryonal rhabdomyosarcoma located in the param..[+] An embryonal rhabdomyosarcoma located in the parameningeal region. [-]
punctate palmoplantar keratoderma	punctate palmoplantar hyperkeratosis; punctate ker.. [+] punctate palmoplantar hyperkeratosis; punctate keratosis palmoplantaris [-]	A palmoplantar keratosis characterized by keratose..[+] A palmoplantar keratosis characterized by keratoses with a raindrop pattern on the palmoplantar surface, skin lesions which may involve the whole of the palmoplantar surface, or may be more restricted in their distribution. [-]
punctate palmoplantar keratoderma type III	punctate palmoplantar hyperkeratosis type 3; punct.. [+] punctate palmoplantar hyperkeratosis type 3; punctate palmoplantar keratoderma type 3; acrokeratoelastoidosis of Costa [-]	A punctate palmoplantar keratoderma that is charac..[+] A punctate palmoplantar keratoderma that is characterized by hyperkeratinization of the palms and soles, has_material_basis_in autosomal dominant inheritance of mutation in the AAGAB gene. [-]
Parkinson's disease 6	PARK6; early-onset Parkinson disease 6; autosomal .. [+] PARK6; early-onset Parkinson disease 6; autosomal recessive early-onset Parkinson disease 6; autosomal recessive early-onset Parkinson's disease 6 [-]	An early-onset Parkinson's disease that has_materi..[+] An early-onset Parkinson's disease that has_material_basis_in mutations in the PINK1 gene on chromosome 1p36.12. [-]
posterior amorphous corneal dystrophy	PACD; chromosome 12q21.33 deletion syndrome	A stromal dystrophy that is characterized by irreg..[+] A stromal dystrophy that is characterized by irregular sheetlike areas of opacification with involvement of the Descemet membrane and, in some instances, alterations of the normal endothelial mosaic and that has_material_basis_in a chromosome 12q21.33 contiguous gene deletion syndrome. [-]
posterior polymorphous corneal dystrophy	PPCD; Schlichting dystrophy; hereditary polymorphu.. [+] PPCD; Schlichting dystrophy; hereditary polymorphus posterior corneal dystrophy [-]	A corneal dystrophy that is characterized by chang..[+] A corneal dystrophy that is characterized by changes in Descemet's membrane and endothelial layer. [-]
Perlman syndrome	nephroblastomatosis - fetal ascites - macrosomia -.. [+] nephroblastomatosis - fetal ascites - macrosomia - Wilms tumor; nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor; renal hamartomas, nephroblastomatosis and fetal gigantism [-]	A syndrome characterized by polyhydramnios with ne..[+] A syndrome characterized by polyhydramnios with neonatal macrosomia, nephromegaly, distinctive facial appearance, renal dysplasia, nephroblastomatosis, and predisposition to Wilms tumor. It shows similarities to Beckwith-Wiedemann syndrome. [-]

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