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681
|
|
|
Succinate dehydrogenase complex iron sulfur subunit B |
CWS2, IP, MC2DN4, PGL4, PPGL4, SDH, SDH1, SDH2, SDHIP |
Adenoma sebaceum, Adrenal gland pheochromocytoma, Anemia, Aniridia, Autism, Brachydactyly, Breast cancer, Breast carcinoma, Cafe-au-lait spot, Hereditary cancer syndrome, Capillary hemangioma of retina, Carcinoma, Carney triad, Carney-stratakis syndrome, Cataract, Colonic neoplasms, Congenital pectus excavatum, Congestive heart failure, Conjunctival hamartoma, Cowden syndrome, Cranial nerve compression, Cranial nerve paralysis, Dementia, Developmental delay, Developmental regression, Disorder of skeletal muscle, Distal amyotrophy, Dwarfism, Dysphagia, Endocrine gland cancer, Endometrial carcinoma, Enlarged polycystic ovaries, Episodic paroxysmal anxiety, Esophagus neoplasm, External ophthalmoplegia, Extra-adrenal paraganglioma, Extra-adrenal pheochromocytoma, Follicular thyroid carcinoma, Gastrointestinal neoplasms, Gastrointestinal stromal tumor, Glomerulonephritis, Glomerulosclerosis, Glomus jugulare tumor, Gynecomastia, Hamartoma, Hamartomatous polyposis, Hearing loss, Hemangioma, Hemangioma, cavernous, Hereditary paraganglioma, Hereditary paraganglioma-pheochromocytoma syndromes, Hereditary pheochromocytoma-paraganglioma, High palate, Hypercalcemia, Hypertension associated with pheochromocytoma, Hypertensive retinopathy, Hypertrophic cardiomyopathy, Impaired cognition, Intestinal neoplasms, Intestinal obstruction, Isolated succinate-coq reductase deficiency, Kidney cancer, Left ventricular hypertrophy, Lipoma, Macrocephaly, Macroglossia, Melanocytic nevus, Melanoma, Meningioma, Mental retardation, Mitochondrial complex deficiency, Mitochondrial diseases, Motor delay, Myoclonic seizures, Myopia, Neoplasms, Neurofibroma, Noncompaction cardiomyopathy, Nystagmus, Palmoplantar keratoderma, Pancreatic adenocarcinoma, Panic disorder, Papilloma, Paraganglioma, Paraganglioma and gastric stromal sarcoma, Paraganglioma of head and neck, Paroxysmal hypertension, Pheochromocytoma, Polyp of large intestine, Pulmonary chondroma, Pulsatile tinnitus, Rectal neoplasms, Renal artery stenosis, Renal carcinoma, Retinitis pigmentosa, Sarcoma, Scoliosis, Sinus tachycardia, Spastic tetraparesis, Stomach neoplasms, Succinate-coenzyme q reductase deficiency, Urticaria, Vesicoureteral reflux, Vocal cord paralysisView all (89 more) |
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682
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|
|
Succinate dehydrogenase complex subunit C |
CYB560, CYBL, PGL3, PPGL3, QPS1, SDH3 |
Adenoma sebaceum, Adrenal gland pheochromocytoma, Anemia, Aniridia, Autism, Brachydactyly, Breast carcinoma, Cafe-au-lait spot, Hereditary cancer syndrome, Capillary hemangioma of retina, Carcinoma, Carney triad, Carney-stratakis syndrome, Cataract, Colonic neoplasms, Congenital pectus excavatum, Congestive heart failure, Conjunctival hamartoma, Cowden syndrome, Cranial nerve compression, Cranial nerve paralysis, Developmental delay, Dwarfism, Dysphagia, Endocrine gland cancer, Endometrial carcinoma, Enlarged polycystic ovaries, Episodic paroxysmal anxiety, Esophagus neoplasm, Extra-adrenal paraganglioma, Extra-adrenal pheochromocytoma, Follicular thyroid carcinoma, Ganglioneuroma, Gastrointestinal neoplasms, Gastrointestinal stromal tumor, Glomerulonephritis, Glomerulosclerosis, Glomus jugulare tumor, Gynecomastia, Hamartoma, Hamartomatous polyposis, Hearing loss, Hemangioma, cavernous, Hereditary paraganglioma-pheochromocytoma syndromes, Hereditary pheochromocytoma-paraganglioma, High palate, Hypercalcemia, Hypertension associated with pheochromocytoma, Hypertensive retinopathy, Impaired cognition, Intestinal neoplasms, Intestinal obstruction, Lipoma, Macrocephaly, Macroglossia, Melanocytic nevus, Melanoma, Meningioma, Mental retardation, Mitochondrial diseases, Myopia, Neurofibroma, Palmoplantar keratoderma, Panic disorder, Papilloma, Paraganglioma, Paraganglioma and gastric stromal sarcoma, Paraganglioma of head and neck, Pheochromocytoma, Polyp of large intestine, Pulmonary chondroma, Pulsatile tinnitus, Rectal neoplasms, Renal carcinoma, Sarcoma, Scoliosis, Sinus tachycardia, Stomach neoplasms, Urticaria, Vocal cord paralysisView all (65 more) |
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683
|
|
|
Solute carrier family 17 member 9 |
C20orf59, POROK8, VNUT |
|
|
684
|
|
|
Succinate dehydrogenase complex subunit D |
CBT1, CII-4, CWS3, MC2DN3, PGL, PGL1, PPGL1, QPs3, SDH4, cybS |
Adenoma sebaceum, Adrenal gland pheochromocytoma, Aniridia, Asthma, Autism, Brachydactyly, Breast carcinoma, Bronchospasm, Cafe-au-lait spot, Hereditary cancer syndrome, Capillary hemangioma of retina, Carcinoid syndrome, Carcinoid tumor of intestine, Carcinoma, Cardiomyopathy, Carney-stratakis syndrome, Carotid body paraganglioma, Cataract, Congenital pectus excavatum, Congestive heart failure, Conjunctival hamartoma, Cowden syndrome, Cranial nerve compression, Cranial nerve paralysis, Dementia, Developmental delay, Developmental regression, Disorder of skeletal muscle, Distal amyotrophy, Dwarfism, Dysphagia, Endocrine gland cancer, Endometrial carcinoma, Enlarged polycystic ovaries, Episodic paroxysmal anxiety, Excessive tearing, External ophthalmoplegia, Extra-adrenal paraganglioma, Extra-adrenal pheochromocytoma, Follicular thyroid carcinoma, Gastrointestinal neoplasms, Gastrointestinal stromal tumor, Glomerulonephritis, Glomerulosclerosis, Glomus jugulare tumor, Glomus tympanicum paraganglioma, Glomus vagale tumor, Gynecomastia, Hamartoma, Hamartomatous polyposis, Hearing loss, Heart failure, Hemangioma, Hemangioma, cavernous, Hereditary paraganglioma-pheochromocytoma syndromes, Hereditary pheochromocytoma-paraganglioma, High palate, Hypercalcemia, Hypertension associated with pheochromocytoma, Hypertensive retinopathy, Hypertrophic cardiomyopathy, Impaired cognition, Intestinal carcinoid, Intestinal obstruction, Isolated succinate-coq reductase deficiency, Left ventricular hypertrophy, Left ventricular noncompaction, Lipoma, Macrocephaly, Macroglossia, Melanocytic nevus, Melanoma, Meningioma, Mental retardation, Merkel cell carcinoma, Mitochondrial cardiomyopathy, Mitochondrial complex deficiency, Mitochondrial diseases, Motor delay, Myoclonic seizures, Myopathy, Myopia, Hypotonia, Neoplasms, Noncompaction cardiomyopathy, Nystagmus, Optic atrophy, Palmoplantar keratoderma, Panic disorder, Papilloma, Paraganglioma, Paraganglioma and gastric stromal sarcoma, Paragangliomas with sensorineural hearing loss, Paraganglioma of head and neck, Paroxysmal hypertension, Pheochromocytoma, Polyp of large intestine, Ptosis, Pulmonary carcinoid tumor, Pulsatile tinnitus, Renal artery stenosis, Renal carcinoma, Retinitis pigmentosa, Scoliosis, Sinus tachycardia, Spastic tetraparesis, Tricuspid valve insufficiency, Ventricular failure, Vesicoureteral reflux, Vocal cord paralysisView all (95 more) |
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685
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|
|
STING1 ER exit protein 1 |
CXorf56, MRX107, STEEP, XLID107 |
Attention deficit hyperactivity disorder, Autism, Developmental delay, Facial paralysis, Neurosensory hearing impairment, Mental retardation, Macrocephaly, Macrotia, Malocclusion, Meckel diverticulum, Mental retardation, x-linked, Non-syndromic intellectual disability, x-linked, Obesity, Seizure, Syndactyly of the toes |
|
686
|
|
|
Selectin E |
CD62E, ELAM, ELAM1, ESEL, LECAM2, selectin-e |
|
|
687
|
|
|
Selectin L |
CD62L, LAM1, LECAM1, LEU8, LNHR, LSEL, LYAM1, PLNHR, TQ1 |
|
|
688
|
|
|
Selectin P |
CD62, CD62P, GMP140, GRMP, LECAM3, PADGEM, PSEL |
|
|
689
|
|
|
Selectin P ligand |
CD162, CLA, PSGL-1, PSGL1 |
|
|
690
|
|
|
Semaphorin 3F |
SEMA-IV, SEMA4, SEMAK |
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