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Disease	Synonyms	Description	Articles	Phenotypes
primary pigmented nodular adrenocortical disease 3	PPNAD3	A primary pigmented nodular adrenocortical disease..[+] A primary pigmented nodular adrenocortical disease that has_material_basis_in heterozygous mutation in the PDE8B gene on chromosome 5q13.3. [-]
primary pigmented nodular adrenocortical disease 4	PPNAD4; chromosome 19p13 duplication syndrome	A primary pigmented nodular adrenocortical disease..[+] A primary pigmented nodular adrenocortical disease that has_material_basis_in duplication on chromosome 19p13 that includes the PRKACA gene. [-]
palmoplantar keratoderma and woolly hair	PPKWH; keratoderma with woolly hair type IV; wooll.. [+] PPKWH; keratoderma with woolly hair type IV; woolly hair-palmoplantar keratoderma syndrome type 4 [-]	A nonepidermolytic palmoplantar keratoderma charac..[+] A nonepidermolytic palmoplantar keratoderma characterized by striate palmoplantar keratoderma, sparse and woolly hair, leukonychia, and the absence of cardiomyopathy symptoms or findings on echocardiography and electrocardiogram that has_material_basis_in homozygous mutation in the KANK2 gene on chromosome 19p13.2. [-]
physical disorder	congenital disorder	A disease that has_material_basis_in a genetic abn..[+] A disease that has_material_basis_in a genetic abnormality, error with embryonic development, infection or compromised intrauterine environment. [-]	163 articles	309 matches
pycnodysostosis		An osteochondrodysplasia that has_material_basis_i..[+] An osteochondrodysplasia that has_material_basis_in a mutation in the CTSK gene which results_in dwarfism, brittle bones, osteopetrosis, shortening of the distal phalanges. [-]
pseudoachondroplasia	pseudoachondroplastic dysplasia; PSEUDOACHONDROPLA.. [+] pseudoachondroplastic dysplasia; PSEUDOACHONDROPLASIA; SPONDYLOEPIPHYSEAL DYSPLASIA, PSEUDOACHONDROPLASTIC [-]	An osteochondrodysplasia that has_material_basis_i..[+] An osteochondrodysplasia that has_material_basis_in mutations in the COMP gene which results_in short limb dwarfism. [-]
PHARC syndrome	polyneyropathy, hearing loss, ataxia, retinitis pi.. [+] polyneyropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract [-]	A syndrome that is characterized by polyneuropathy..[+] A syndrome that is characterized by polyneuropathy, hearing loss, cerebellar ataxia, retinitis pigmentosa and early-onset cataract. [-]
PTEN hamartoma tumor syndrome		A syndrome characterized as a spectrum of disorder..[+] A syndrome characterized as a spectrum of disorders (Cowden syndrome, Bannayan-Riley-Ruvalcaba syndrome, PTEN-related Proteus syndrome, and Proteus-like syndrome) caused by germline mutations of the PTEN gene. [-]
Peters plus syndrome	Peters-plus syndrome; Peters anomaly-short limb dw.. [+] Peters-plus syndrome; Peters anomaly-short limb dwarfism syndrome; Krause-Kivlin syndrome [-]	A syndrome that is characterized by anterior chamb..[+] A syndrome that is characterized by anterior chamber eye anomalies, short limbs with broad distal extremities, characteristic facial features, cleft lip/palate, and variable developmental delay/intellectual disability. [-]
primary mediastinal B-cell lymphoma	Primary mediastinal clear cell lymphoma of B-cell .. [+] Primary mediastinal clear cell lymphoma of B-cell type; Large cell lymphoma of the mediastinum; Mediastinal diffuse large-cell lymphoma with sclerosis [-]	A large B-cell lymphoma that is is characterized b..[+] A large B-cell lymphoma that is is characterized by a diffuse proliferation of medium to large B-cells associated with sclerosis. [-]
polycystic kidney disease 4		A autosomal recessive polycystic kidney disease th..[+] A autosomal recessive polycystic kidney disease that has_material_basis_in mutation in the PKD4 gene. [-]
punctate palmoplantar keratoderma type II		A punctate palmoplantar keratoderma that is charac..[+] A punctate palmoplantar keratoderma that is characterized by multiple, asymptomatic, 1 to 2 mm-long, firm, hyperkeratotic projections on the palms, soles and digits. [-]
punctate palmoplantar keratoderma type I	punctate palmoplantar keratoderma type 1B; punctat.. [+] punctate palmoplantar keratoderma type 1B; punctate palmoplantar keratoderma type 1A [-]	A punctate palmoplantar keratoderma that is charac..[+] A punctate palmoplantar keratoderma that is characterized by multiple hyperkeratotic centrally indented papules that develop in early adolescence or later and are irregularly distributed on the palms and soles. [-]
primary spontaneous pneumothorax		A pneumothorax that is characterized by an abnorma..[+] A pneumothorax that is characterized by an abnormal accumulation of air in the space between the lungs and the chest cavity that can result in the partial or complete collapse of a lung. [-]
pseudohypoparathyroidism type IB		A pseudohypoparathyroidism characterized by isolat..[+] A pseudohypoparathyroidism characterized by isolated renal parathyroid hormone (PTH) resistance resulting in hypocalcemia, hyperphosphatemia and elevated PTH levels that has_material_basis_in mutations that alter the methylation pattern of GNAS on 20q13.32. [-]
Perrault syndrome 6		A Perrault syndrome that is characterized by senso..[+] A Perrault syndrome that is characterized by sensorineural deafness in both males and females, with females also presenting with ovarian dysgenesis resulting in amenorrhea and infertility and that has_material_basis_in homozygous mutation in the ERAL1 gene on chromosome 17q11. [-]
primary ciliary dyskinesia 37		A primary ciliary dyskinesia that has_material_bas..[+] A primary ciliary dyskinesia that has_material_basis_in homozygous mutation in the DNAH1 gene on chromosome 3p21. [-]
polycystic kidney disease 5		A autosomal recessive polycystic kidney disease th..[+] A autosomal recessive polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of homozygous mutation in the DZIP1L gene on chromosome 3q22. [-]
peripheral nervous system benign neoplasm		A central nervous system benign neoplasm the is lo..[+] A central nervous system benign neoplasm the is located_in the peripheral nervous system. [-]
polycystic kidney disease		A cystic kidney disease that is characterized by t..[+] A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure. [-]	14 articles
Phelan-McDermid syndrome	22q13.3 deletion syndrome; monosomy 22q13 syndrome.. [+] 22q13.3 deletion syndrome; monosomy 22q13 syndrome [-]	A chromosomal deletion syndrome that has_material_..[+] A chromosomal deletion syndrome that has_material_basis_in a deletion, translocation, ring chromosome formation or other structural change of the terminal end of chromosome 22 in the 22q13 region or a disease-causing mutation of the SHANK3 gene and that is characterized by neonatal hypotonia, absent to severely delayed speech, global developmental delay, and minor dysmorphic facial features. Most cases of 22q13.3 deletion syndrome are not inherited with 20% of cases (autosomal dominant) inherited from a parent. The deletion occurs most often as a random event during the formation of reproductive cells (eggs or sperm) or in early fetal development. [-]
peroxisomal biogenesis disorder		A peroxisomal biogenesis disorder that has_materia..[+] A peroxisomal biogenesis disorder that has_material_basis_in defects in PEX genes. [-]
pustular psoriasis 14	acrodermatitis continua of Hallopeau; deficiency o.. [+] acrodermatitis continua of Hallopeau; deficiency of IL-36R antagonist [-]	A psoriasis characterized by sudden, repeated epis..[+] A psoriasis characterized by sudden, repeated episodes of high-grade fever, generalized rash, and disseminated pustules, with hyperleukocytosis and elevated serum levels of C-reactive protein that has_material_basis_in homozygous or compound heterozygous mutation in the IL36RN gene on chromosome 2q14. [-]
psoriasis 2		A psoriasis that has_material_basis_in heterozygou..[+] A psoriasis that has_material_basis_in heterozygous mutation in the CARD14 gene on chromosome 17q25. [-]
peroxisome biogenesis disorder 1A	peroxisome biogenesis disorder 1A (Zellweger)	A Zellweger syndrome that has_material_basis_in ho..[+] A Zellweger syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the PEX1 gene on chromosome 7q21. [-]
peroxisome biogenesis disorder 2A	peroxisome biogenesis disorder 2A (Zellweger)	A Zellweger syndrome that has_material_basis_in ho..[+] A Zellweger syndrome that has_material_basis_in homozygous mutation in the PEX5 gene on chromosome 12p13. [-]
peroxisome biogenesis disorder 3A	peroxisome biogenesis disorder 3A (Zellweger)	A Zellweger syndrome that has_material_basis_in ho..[+] A Zellweger syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the PEX12 gene on chromosome 17. [-]
peroxisome biogenesis disorder 4A	peroxisome biogenesis disorder 4A (Zellweger)	A Zellweger syndrome that has_material_basis_in ho..[+] A Zellweger syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the PEX6 gene on chromosome 6p21.1. [-]
peroxisome biogenesis disorder 5A	peroxisome biogenesis disorder 5A (Zellweger)	A Zellweger syndrome that has_material_basis_in ho..[+] A Zellweger syndrome that has_material_basis_in homozygous mutation in the PEX2 gene on chromosome 8q21. [-]
peroxisome biogenesis disorder 6A	peroxisome biogenesis disorder 6A (Zellweger)	A Zellweger syndrome that has_material_basis_in ho..[+] A Zellweger syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the PEX10 gene on chromosome 1p36. [-]
peroxisome biogenesis disorder 7A	peroxisome biogenesis disorder 7A (Zellweger)	A Zellweger syndrome that has_material_basis_in ho..[+] A Zellweger syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the PEX26 gene on chromosome 22q11. [-]
peroxisome biogenesis disorder 8A	peroxisome biogenesis disorder 8A (Zellweger)	A Zellweger syndrome that has_material_basis_in ho..[+] A Zellweger syndrome that has_material_basis_in homozygous mutation in the PEX16 gene on chromosome 11p11. [-]
peroxisome biogenesis disorder 10A	peroxisome biogenesis disorder 10A (Zellweger)	A Zellweger syndrome that has_material_basis_in ho..[+] A Zellweger syndrome that has_material_basis_in homozygous mutation in the PEX3 gene on chromosome 6q24. [-]
peroxisome biogenesis disorder 11A	peroxisome biogenesis disorder 11A (Zellweger)	A Zellweger syndrome that has_material_basis_in ho..[+] A Zellweger syndrome that has_material_basis_in homozygous mutation in the PEX13 gene on chromosome 2p15. [-]
peroxisome biogenesis disorder 12A	peroxisome biogenesis disorder 12A (Zellweger)	A Zellweger syndrome that has_material_basis_in ho..[+] A Zellweger syndrome that has_material_basis_in homozygous mutation in the PEX19 gene on chromosome 1q23. [-]
peroxisome biogenesis disorder 13A	peroxisome biogenesis disorder 13A (Zellweger)	A Zellweger syndrome that has_material_basis_in ho..[+] A Zellweger syndrome that has_material_basis_in homozygous mutation in the PEX14 gene on chromosome 1p36. [-]
Parkinson's disease 22	autosomal dominant Parkinson's disease 22	A late onset Parkinson's disease that has_material..[+] A late onset Parkinson's disease that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the coiled-coil-helix-coiled-coil-helix domain containing 2 gene on chromosome 7p11.2. [-]
PAPA syndrome	pyogenic arthritis, pyoderma gangrenosum and acne; .. [+] pyogenic arthritis, pyoderma gangrenosum and acne [-]	A syndrome that is characterized by pyoderma gangr..[+] A syndrome that is characterized by pyoderma gangrenosum, pyogenic arthritis, acne and suppurative hidradenitis and heterozygous mutation in the PSTPIP1 gene on chromosome 15q24. [-]
PEHO syndrome		A brain disease that is characterized by extreme c..[+] A brain disease that is characterized by extreme cerebellar atrophy due to almost total granule neuron loss. [-]
peroxisome biogenesis disorder 2B		A peroxisomal biogenesis disorder that has_materia..[+] A peroxisomal biogenesis disorder that has_material_basis_in homozygous mutation in the PEX5 gene on chromosome 12p13.3. [-]
posterior polymorphous corneal dystrophy 4		A posterior polymorphous corneal dystrophy that is..[+] A posterior polymorphous corneal dystrophy that is characterized by an irregular posterior corneal surface with occasional opacities of variable size and shape and that has_material_basis_in heterozygous mutation in the GRHL2 gene on chromosome 8q22. [-]
prothrombin thrombophilia		A thrombophilia that is characterized by increases..[+] A thrombophilia that is characterized by increases the risk of blood clots including deep vein thrombosis and pulmonary embolism and that has_material_basis_in heterozygous mutation in the thrombin gene (F2 gene) on chromosome 11p11. [-]
polymyositis		A myositis that is characterized by muscle weaknes..[+] A myositis that is characterized by muscle weakness affecting both sides of your body. [-]
pyridoxine-dependent epilepsy		An epilepsy that is characterized by intractable s..[+] An epilepsy that is characterized by intractable seizures within the first weeks to months of life that are not controlled with antiepileptic drugs but respond both clinically and electrographically to large daily supplements of pyridoxine. [-]
partial androgen insensitivity syndrome	Reifenstein syndrome	An androgen insensitivity syndrome that is charact..[+] An androgen insensitivity syndrome that is characterized by a 46,XY karyotype and testes that produce age-appropriate androgen levels but have undermasculinized external genitalia due to defects in androgen action. [-]
plasmablastic lymphoma		A large B-cell lymphoma that is characterized by t..[+] A large B-cell lymphoma that is characterized by the presence of large neoplastic cells resembling B-immunoblasts which have the immunophenotypic profile of plasma cells. [-]
proximal symphalangism 1		A proximal symphalangism that is characterized by ..[+] A proximal symphalangism that is characterized by ankylosis of the proximal interphalangeal joints, carpal and tarsal bone fusion, and, in some cases, conductive deafness and that has_material_basis_in heterozygous mutation in the NOG gene on chromosome 17q22. [-]
proximal symphalangism 2		A proximal symphalangism that is characterized by ..[+] A proximal symphalangism that is characterized by absence of the cuboid bone and lack of shortness of the first and fifth metacarpal bones, and the presence of distal interphalangeal joint fusions and flat feet and that has_material_basis_in heterozygous mutation in the GDF5 gene on chromosome 20q11. [-]
persistent mild asthma		A chronic asthma that is characterized by severity..[+] A chronic asthma that is characterized by severity with symptoms two or more days per week, nighttime awakenings three to four times per month, use of short-acting beta agonist for symptom control two or more days per week and minor limitation of normal activity. [-]
persistent moderate asthma		A chronic asthma that is characterized by severity..[+] A chronic asthma that is characterized by severity with daily symptoms, nighttime awakenings more than once per week, daily use of short-acting beta agonist for symptom control and some limitation of normal activity. [-]

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