|
711
|
|
|
Proteinase 3 |
ACPA, AGP7, C-ANCA, CANCA, MBN, MBT, NP-4, NP4, P29, PR-3, PR3 |
Chronic obstructive pulmonary disease, Cranial nerve paralysis, Diabetes insipidus, Gangrene, Granulomatosis, Granulomatosis with polyangiitis, Hearing loss, Hydronephrosis, Hypertension, Inflammatory abnormality of the eye, Intestinal obstruction, Myeloid leukemia, Otitis media, Pancreatitis, Pericarditis, Pleuritis, Proptosis, Prostatitis, Pulmonary fibrosis, Renal glomerular disease, Renal insufficiency, Retinal diseases, Sensory neuropathy, Sinusitis, VasculitisView all (10 more) |
|
712
|
|
|
Prosaposin |
GLBA, PARK24, PSAPD, SAP1, SAP2 |
Anemia, Asthma, Bowel incontinence, Central nervous system demyelination, Cholecystitis, Clonic seizures, Combined saposin deficiency, Delusions, Dementia, Developmental delay, Developmental regression, Dysarthria, Dysphagia, Encephalopathy, Neoplasm of gallbladder, Gaucher disease, Hallucinations, Hypoplasia of corpus callosum, Krabbe disease, Leukodystrophy, Mental depression, Metachromatic leukodystrophy, Mood swings, Movement disorders, Optic atrophy, Osteopenia, Polyneuropathy, Respiratory failure, Schizophrenia, Seizure, Sensorineural hearing loss, Sleep apnea, Spastic tetraparesis, Sphingolipid activator protein 1 deficiencyView all (19 more) |
|
713
|
|
|
Pleckstrin and Sec7 domain containing |
EFA6, EFA6A, PSD1, TYL |
|
|
714
|
|
|
Presenilin 1 |
ACNINV3, AD3, CMD1U, FAD, PS-1, PS1, PSNL1, S182 |
Abulia, Acne inversa, Alexia, Alzheimer disease, Alzheimer disease, with spastic paraparesis and apraxia, Amyloidosis, Amyotrophic lateral sclerosis, Anomia, Anxiety disorder, Aphasia, Apraxia, Behavioral variant of frontotemporal dementia, Brain atrophy, Broca aphasia, Cardiomyopathy, Cerebellar atrophy, Cerebral atrophy, Cerebral cortical atrophy, Cognitive disorder, Compulsive hoarding, Congestive heart failure, Degenerative diseases, central nervous system, Dementia, Dementia of frontal lobe, Dilated cardiomyopathy, Dysarthria, Dyscalculia, Dysgraphia, Dyslexia, Dysphagia, Dysphasia, Elbow flexion contracture, Frontotemporal cerebral atrophy, Frontotemporal dementia, Grammar-specific speech disorder, Hallucinations, Hearing loss, Hidradenitis suppurativa, High palate, Language disorders, Learning disorders, Lipoatrophy, Lipodystrophy, Memory disorders, Age-related memory disorders, Mental depression, Mental retardation, Myocardial diseases, Myopathy, Neurodegenerative disorders, Oculomotor apraxia, Oculovestibuloauditory syndrome, Palmoplantar keratoderma, Parkinson disease, Perifolliculitis, Pica, Postnatal asphyxia, Nonfluent aphasia, Progressive non-fluent aphasia, Psychosis, Seizure, Semantic dementia, Senile dementia, Senile plaques, Shoulder flexion contracture, Spastic tetraparesis, Stereotyped behavior, Temporal cortical atrophyView all (53 more) |
|
715
|
|
|
Presenilin 2 |
AD3L, AD4, CMD1V, PS2, STM2 |
Alzheimer disease, Anxiety disorder, Aphasia, Bipolar disorder, Cardiomyopathy, Cerebral amyloid angiopathy, Cerebral cortical atrophy, Congestive heart failure, Dementia, Dilated cardiomyopathy, Dysgraphia, Hallucinations, Hearing loss, Huntington disease-like, Language disorders, Lipoatrophy, Lipodystrophy, Mental retardation, Myopathy, Oculomotor apraxia, Oculovestibuloauditory syndrome, Palmoplantar keratoderma, Parkinson disease, Postnatal asphyxia, Schizophrenia, Semantic dementia, Senile dementia, Senile plaquesView all (13 more) |
|
716
|
|
|
Pannexin 2 |
PX2, hPANX2 |
|
|
717
|
|
|
Pregnancy specific beta-1-glycoprotein 5 |
FL-NCA-3, PSG |
|
|
718
|
|
|
Pregnancy specific beta-1-glycoprotein 11 |
PSBG-11, PSBG-13, PSG13, PSG14 |
|
|
719
|
|
|
Proteasome 20S subunit alpha 2 |
HC3, MU, PMSA2, PSC2 |
|
|
720
|
|
|
Proteasome 20S subunit alpha 3 |
HC8, PSC3 |
|
