Genes | GeDiPNet - Gene Disease Pathway & Associations

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9791 to 9800 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
9791	23035	PHLPP2	PH domain and leucine rich repeat protein phosphatase 2	PHLPPL, PPM3B	Post-operative acute kidney injury, Prostate cancer
9792	162466	PHOSPHO1	Phosphoethanolamine/phosphocholine phosphatase 1	-	Bone disease, Metabolic bone disorder
9793	401	PHOX2A	Paired like homeobox 2A	ARIX, CFEOM2, FEOM2, NCAM2, PMX2A	Congenital fibrosis of extraocular muscles
9794	8929	PHOX2B	Paired like homeobox 2B	CCHS, NBLST2, NBPhox, PMX2B	Haddad syndrome, Central hypoventilation syndrome, Congenital central hypoventilation syndrome, Crohn disease, Hirschsprung disease, Neuroblastoma, Schizophrenia
9795	57661	PHRF1	PHD and ring finger domains 1	PPP1R125, RNF221	Hirschsprung disease, Hypothyroidism, Systemic lupus erythematosus, Rheumatoid arthritis, Systemic sclerosis
9796	10745	PHTF1	Putative homeodomain transcription factor 1	PHTF	Ankylosing spondylitis, Anti-neutrophil antibody associated vasculitis, Asthma, Autoimmune disease, Autoimmune thyroid disease, Basal cell carcinoma, Celiac disease, Common variable immunodeficiency, Crohn disease, Diabetic ketoacidosis, Hyperthyroidism, Hypothyroidism, Inflammatory bowel disease, Juvenile idiopathic arthritis, Keratinocyte carcinoma View all (17 more)
9797	57157	PHTF2	Putative homeodomain transcription factor 2	-	Atrial fibrillation, Cardioembolic stroke, Dental caries, Hypertension, Major depressive disorder, Obesity
9798	5264	PHYH	Phytanoyl-CoA 2-hydroxylase	LN1, LNAP1, PAHX, PHYH1, RD	Refsum disease, Optic atrophy, Orofacial cleft, Peroxisomal disorder, Retinitis pigmentosa
9799	9796	PHYHIP	Phytanoyl-CoA 2-hydroxylase interacting protein	DYRK1AP3, PAHX-AP, PAHXAP1	Hypertriglyceridemia
9800	85007	PHYKPL	5-phosphohydroxy-L-lysine phospho-lyase	AGXT2L2, PHLU	Dental caries, Glomerulonephritis, Ulcerative colitis

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