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List of all diseases starting with P

• PAICS DEFICIENCY MIM=
• PARKINSONISM-DYSTONIA, INFANTILE, 1; PKDYS1 MIM=613135
• PARKINSONISM-DYSTONIA, INFANTILE, 2; PKDYS2 MIM=618049
• PATENT DUCTUS VENOSUS MIM=601466
• PEARSON SYNDROM (PS) MIM=557000
• PEDIATRIC CATARACT [DD] MIM=
• PELIZAEUS MERZBACHER DISEASE MIM=312080
• PENDRED SYNDROME (PDS) MIM=274600
• PENTOSURIA; ESSENTIAL BENIGN PENTOSURIA MIM=260800
• PEROXISOMAL DISORDERS, NEW TYPE, LIVER MIM=
• PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) MIM=214100
• PEROXISOME BIOGENESIS DISORDER 1B (PBD1B, NALD) MIM=601539
• PEROXISOME BIOGENESIS DISORDER 2B (PBD2B) MIM=202370
• PEROXISOME BIOGENESIS DISORDER 3A (PBD3A) MIM=614859
• PEROXISOME BIOGENESIS DISORDER 3B (PBD3B) MIM=266510
• PEROXISOME BIOGENESIS DISORDER 4B (PBD4B) MIM=614863
• PET117 CYTOCHROME c OXIDASE CHAPERONE; PET117 MIM=614771
• PHENYLKETONURIA (PKU) MIM=261600
• PHENYLKETONURIA, FETAL EFFECTS FROM MATERNAL (MPKU) MIM=261600
• PHOSPHATIDYLINOSITOL 4-KINASE TYPE 2 ALPHA DEFICIENCY (PI4K2A) MIM=609763
• PHOSPHATIDYLINOSITOL GLYCAN ANCHOR BIOSYNTHESIS CLASS B PROTEIN (PIGB) MIM=604122
• PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY 1, CYTOSOLIC (PEPCK1) MIM=261680
• PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, MITOCHONDRIAL (PEPCK2) MIM=261650
• PHOSPHOGLYCERATE KINASE 1 DEFICIENCY MIM=300653
• PHOSPHOHYDROXYLYSINURIA (PHLU) MIM=615011
• PHOSPHORIBOSYL PYROPHOSPHATE SYNTHETASE I DEFECT (CMTX5) MIM=311070
• PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE SUPERACTIVITY (PRPPS) MIM=300661
• PHOSPHOSERINE AMINOTRANSFERASE DEFICIENCY MIM=610992
• PHOSPHOSERINE PHOSPHATASE DEFICIENCY (PSPH) MIM=614023
• PITUITARY HORMONE DEFICIENCY, COMBINED, 1; CPHD1 MIM=613038
• PITUITARY HORMONE DEFICIENCY, COMBINED, 2; CPHD2 MIM=262600
• PITUITARY HORMONE DEFICIENCY, COMBINED, 3; CPHD3 MIM=221750
• PITUITARY HORMONE DEFICIENCY, COMBINED, 4; CPHD4 MIM=262700
• PITUITARY STALK INTERRUPTION SYNDROME (PSIS) MIM=
• POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY (PGBM1) MIM=615895
• PORPHYRIA CUTANEA TARDA, TYPE I (PCT) MIM=176090
• PORPHYRIA CUTANEA TARDA, TYPE II (HEP) MIM=176100
• PORPHYRIA VARIEGATA (VP) MIM=176200
• PREMATURE INFANTS, BRONCHOPULMONARY DYSPLASIA (BPD) [DD] MIM=
• PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES (PASNA) MIM=615474
• PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS (PEO) MIM=258450
• PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 6 (PEOA6) MIM=615156
• PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2 (PEOB2) MIM=616479
• PROLIDASE DEFICIENCY MIM=170100
• PROPIONIC ACIDEMIA (PA, PCCA) MIM=606054
• PROPIONIC ACIDEMIA (PA, PCCB) MIM=606054
• PROPROTEIN CONVERTASE 1/3 DEFICIENCY MIM=600955
• PROTOPORPHYRIA, ERYTHROPOIETIC (EPP) MIM=177000
• PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED (XLEPP) MIM=300752
• PSEUDO ZELLWEGER -> D-BIFUNCTIONAL PROTEIN DEFICIENCY MIM=261515
• PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT (PHA1A) MIM=177735
• PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE; PHA1B MIM=264350
• PSEUDOHYPOALDOSTERONISM, TYPE IIA (PHA2A) MIM=145260
• PSEUDOHYPOALDOSTERONISM, TYPE IIB (PHA2B) MIM=614491
• PSEUDOHYPOALDOSTERONISM, TYPE IIC (PHA2C) MIM=614492
• PSEUDOHYPOALDOSTERONISM, TYPE IID (PHA2D) MIM=614495
• PSEUDOHYPOALDOSTERONISM, TYPE IIE (PHA2E) MIM=614496
• PSEUDONEONATAL ADRENOLEUKODYSTROPHY MIM=264470
• PULMONARY HEMOSIDEROSIS MIM=178550
• PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY (PNP) MIM=613179
• PYRIDOXAMINE 5-PRIME-PHOSPHATE OXIDASE DEFICIENCY (PNPO) MIM=610090
• PYRUVATE CARBOXYLASE DEFICIENCY (PC) MIM=266150
• PYRUVATE DEHYDROGENASE DEFICIENCY (E1); PDC MIM=312170
• PYRUVATE DEHYDROGENASE DEFICIENCY (E2) MIM=245348
• PYRUVATE DEHYDROGENASE E1-BETA DEFICIENCY; PDHBD MIM=614111
• PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY MIM=245349
• PYRUVATE DEHYDROGENASE PHOSPHATASE DEFICIENCY; PDHPD MIM=608782
• PYRUVATE KINASE DEFICIENCY MIM=266200