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Disease	Synonyms	Description
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. [-]
pulmonary artery disease		An artery disease that is located in the lungs.
pervasive developmental disorder	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. [-]
paraphilia disorder		n_a
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. [-]
primary cutaneous T-cell non-Hodgkin lymphoma	cutaneous T-cell lymphoma; cutaneous T cell lympho.. [+] cutaneous T-cell lymphoma; cutaneous T cell lymphoma [-]	A non-Hodgkin's lymphoma that has_material_basis_i..[+] A non-Hodgkin's lymphoma that has_material_basis_in a mutation of T cells. [-]
pyridoxine-refractory autosomal recessive sideroblastic anemia		n_a
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. [-]
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. [-]
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		n_a
pontocerebellar hypoplasia	PCH	n_a
pontocerebellar hypoplasia type 1A		n_a
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		n_a
pontocerebellar hypoplasia type 2B		n_a
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		n_a
pontocerebellar hypoplasia type 2E		n_a
pontocerebellar hypoplasia type 3		n_a
pontocerebellar hypoplasia type 4		n_a
pontocerebellar hypoplasia type 5		n_a
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		A pontocerebellar hypoplasia that is characterized..[+] A pontocerebellar hypoplasia that is characterized by delayed psychomotor development, chorea, hypotonia, spasticity and visual defects, has_material_basis_in autosomal recessive inheritance of mutation in the CHMP1A gene. [-]
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		n_a
peeling skin syndrome		A skin disease that is characterized by the painle..[+] A skin disease that is characterized by the painless peeling of the top layer of skin predominately on the hands and feet, has_material_basis_in autosomal recessive inheritance of mutation in the TGM5 gene and/pr CSTA gene. [-]
paroxysmal nocturnal hemoglobinuria		n_a
parietal foramina	Caitlin marks; enlarged parietal foramina; heredit.. [+] Caitlin marks; enlarged parietal foramina; hereditary cranium bifidum [-]	n_a
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 keratoderma type 3; punctate.. [+] punctate palmoplantar keratoderma type 3; punctate palmoplantar hyperkeratosis type 3; acrokeratoelastoidosis of Costa [-]	n_a
Parkinson's disease 2	autosomal recessive juvenile Parkinson disease 2; .. [+] autosomal recessive juvenile Parkinson disease 2; autosomal recessive juvenile Parkinson's disease 2 [-]	An early-onset Parkinson's disease that has_materi..[+] An early-onset Parkinson's disease that has_material_basis_in mutation in the parkin gene on chromosome 6q25.2-q27. [-]
Parkinson's disease 7	autosomal recessive early-onset Parkinson disease .. [+] autosomal recessive early-onset Parkinson disease 7; autosomal recessive early-onset Parkinson's disease 7 [-]	An early-onset Parkinson's disease that has_materi..[+] An early-onset Parkinson's disease that has_material_basis_in homozygous or compound heterozygous mutation in the DJ1 gene on chromosome 1p36. [-]

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