10551
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|
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Patched 1 |
BCNS, BCNS1, NBCCS, PTC, PTC1, PTCH, SLC65B1 |
Anophthalmia/microphthalmia-esophageal atresia syndrome, Asthma, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Basal cell carcinoma, Basal cell nevus syndrome, Brain neoplasms, Breast cancer, Cataract, Obstructive pulmonary disease, Cleft lip, Cleft palate, Complete unilateral cleft lip, Congenital heart disease, Congenital hydrocephalus, Craniofacial abnormalities, Craniosynostosis, Dental caries, Estrogen-receptor negative breast cancer, Fraser syndrome, Gastrointestinal stromal tumor, Gorlin syndrome, Holoprosencephaly, Intellectual developmental disorder, Anterior segment dysgenesis, Major depressive disorder, Medulloblastoma, Microform holoprosencephaly, Syntelencephaly, Migraine, Myopia, Neurotic disorder, Osteoarthritis, Pancreatic neoplasms, Pancreatitis, Pituitary stalk interruption syndrome, Polydactyly, Rhabdomyosarcoma, Rieger syndrome, Schizoaffective disorder, Scoliosis, Semilobar holoprosencephaly, Septopreoptic holoprosencephaly, Skin neoplasms, Small vessel stroke, Turner syndrome, Diabetes mellitus type 2View all (33 more) |
10552
|
|
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Patched 2 |
PTC2, SLC65B2 |
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10553
|
|
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Patched domain containing 1 |
AUTSX4, CXDELp22.11, DELXP22.11, SLC65C1 |
Atrial fibrillation, Autism, Autism, x-linked, Cardiac arrhythmia, Developmental disability, Intellectual developmental disorder, Intellectual developmental disorder, x-linked, Neurodevelopmental disorder, X-linked intellectual disability, Depression |
10554
|
|
|
Patched domain containing 3 (gene/pseudogene) |
PTR, SLC65C3 |
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10555
|
|
|
Patched domain containing 4 |
C6orf138, PTCH53, SLC65C2, dJ402H5.2 |
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10556
|
|
|
Pre T cell antigen receptor alpha |
IMD126, PT-ALPHA, PTA |
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10557
|
|
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Phosphatidylserine synthase 1 |
LMHD, PSS1, PSSA |
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10558
|
|
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Phosphatidylserine synthase 2 |
PSS2 |
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10559
|
|
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Phosphatase and tensin homolog |
10q23del, BZS, CWS1, DEC, GLM2, MHAM, MMAC1, PTEN1, PTENbeta, PTENgama, TEP1 |
Activated pi3k-delta syndrome, Anisometropia, Asthma, Endometrial hyperplasia, Autism, Breast neoplasms, Carcinoma, Adenoid cystic carcinoma, Ductal carcinoma, Hepatocellular carcinoma, Renal cell carcinoma, Cholangiocarcinoma, Concussion, Congenital neurologic anomalies, Cowden disease, Craniofacial abnormalities, Dermatologic disorder, Developmental coordination disorder, Developmental disability, Endometrial neoplasms, Endometriosis, Developmental and epileptic encephalopathy, Meningioma, Prostate cancer, Fatty liver, Fatty liver, alcoholic, Glioma, Global developmental delay, Hemimegalencephaly, Hereditary breast and ovarian cancer syndrome, Hypertension, Hypertrophy, Diabetes mellitus type 2, Intellectual developmental disorder, Language development disorders, Leiomyosarcoma, Leopard syndrome, Leukemia, Lipoma, Lipomatosis, Liver cirrhosis, Long qt syndrome, Lung neoplasms, Lymphoma, Melanoma, Motor skills disorder, Nasopharyngeal carcinoma, Neurodevelopmental disorder, Nonalcoholic fatty liver disease, Ovarian neoplasms, Pancreatic neoplasms, Periodontitis, Polydactyly, Prostatic intraepithelial neoplasia, Prostatic neoplasms, Schizophrenia, Sezary syndrome, Skin disease, Small cell lung carcinoma, Squamous cell carcinoma, Vacterl association, Retinal vasculopathy with cerebral leukodystrophyView all (47 more) |
10560
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|
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Phosphotriesterase related |
HPHRP, RPR-1 |
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