Disease Browser
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Parent Node: Acid-Base Imbalance (D000137) | Parent Node: Anemia, Hemolytic, Congenital (D000745) | Parent Node: Metabolism, Inborn Errors (D008661) | ..Starting node ..Stomatocytosis I (C566111)
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Sister Nodes: | ..3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency (C567784)
| ..3-Hydroxyacyl-CoA Dehydrogenase Deficiency (C535310)
| ..3-Methylglutaconic Aciduria (C579867)
| ..3-Methylglutaconic Aciduria Type IV (C565393)
| ..3-Methylglutaconic Aciduria, Type I (C562801)
| ..3-Methylglutaconic Aciduria, Type V (C565706)
| ..5-Nucleotidase syndrome (C535321)
| ..6-Phosphogluconolactonase Deficiency (C566803)
| ..Acetylcarnitine deficiency (C536006)
| ..Acholinesterasemia (C566750)
| ..Acid Phosphatase Deficiency (C562645)
| ..Adenine phosphoribosyltransferase deficiency (C538228)
| ..AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY (OMIM:608688)
| ..alpha-Fetoprotein Deficiency (C566300)
| ..Amino Acid Metabolism, Inborn Errors (D000592) 169
| ..Amino Acid Transport Disorders, Inborn (D020157) 3
| ..Amobarbital, Deficient N-Hydroxylation of (C565959)
| ..Amyloidosis, Familial (D028226) 13
| ..Arene Oxide Detoxification Defect (C565043)
| ..Aromatase deficiency (C537436)
| ..Aryl Hydrocarbon Hydroxylase Inducibility (C566250)
| ..BISPHOSPHOGLYCERATE MUTASE DEFICIENCY (OMIM:222800)
| ..Brain Diseases, Metabolic, Inborn (D020739) 218
| ..Butyrylcholinesterase deficiency (C537417)
| ..Butyrylcholinesterase Deficiency, Fluoride-Resistant, Japanese Type (C566751)
| ..Carbohydrate Metabolism, Inborn Errors (D002239) 169
| ..Carnitine Acetyltransferase Deficiency (C563249)
| ..Carnitine palmitoyl transferase 2 deficiency (C535589)
| ..Chromate Resistance (C566125)
| ..COENZYME Q10 DEFICIENCY, PRIMARY, 1 (OMIM:607426)
| ..Combined Malonic and Methylmalonic Aciduria (C580002)
| ..Combined Oxidative Phosphorylation Deficiency 1 (C563797)
| ..Combined Oxidative Phosphorylation Deficiency 4 (C565690)
| ..Combined Oxidative Phosphorylation Deficiency 5 (C567126)
| ..Congenital chloride diarrhea (C536210)
| ..Copper deficiency, familial benign (C535468)
| ..Costeff optic atrophy syndrome (C535311)
| ..Coumarin Resistance (C563039)
| ..Coumarin Sensitivity (C567276)
| ..CREATINE PHOSPHOKINASE, ELEVATED SERUM (OMIM:123320)
| ..Cytochrome-c Oxidase Deficiency (D030401) 2
| ..Deafness hyperuricemia neurologic ataxia (C535995)
| ..Deoxyribose-5-Phosphate Aldolase Deficiency (C565112)
| ..Diarrhea 3, Secretory Sodium, Congenital (C562576)
| ..Diarrhea 3, Secretory Sodium, Congenital, Syndromic (C567490)
| ..Diarrhea, Glucose-Stimulated Secretory, with Common Variable Immunodeficiency (C565099)
| ..Dihydropyrimidinase Deficiency (C562815)
| ..Diphenylhydantoin, Defect in Hydroxylation of (C565044)
| ..Drug Metabolism, Poor, CYP2C19-Related (C563703)
| ..Drug Metabolism, Poor, CYP2D6-Related (C563835)
| ..Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency (C562657)
| ..Enterokinase Deficiency (C562649)
| ..Ethanolaminosis (C562651)
| ..Familial gynecomastia, due to increased aromatase activity (C000591739)
| ..Finnish lethal neonatal metabolic syndrome (C537934)
| ..Fumaric aciduria (C538191)
| ..Glucocorticoid Receptor Deficiency (C564221)
| ..Glutamate formiminotransferase deficiency (C537425)
| ..Glycoprotein Storage Disease (C565538)
| ..Glyoxalase II Deficiency (C564215)
| ..Growth Factors, Combined Defect of (C565529)
| ..HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY (OMIM:613470)
| ..HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY (OMIM:235700)
| ..Hyaluronan Metabolism, Defect in (C565742)
| ..Hyperbilirubinemia, Hereditary (D006933) 7
| ..Hypercalcemia, Idiopathic, of Infancy (C562581)
| ..HYPERCHLORHIDROSIS, ISOLATED (OMIM:143860)
| ..Hypoadiponectinemia (C567258)
| ..Hypokalemia, Familial (C562654)
| ..Hypoproteinemia, Hypercatabolic (C565476)
| ..Inosine Triphosphatase Deficiency (C564127)
| ..Intrinsic Factor and R Binder, Combined Congenital Deficiency of (C565461)
| ..Kallikrein, Decreased Urinary Activity of (C563653)
| ..L-Gulonolactone Oxidase, Nonfunctional (C565486)
| ..Lactate Dehydrogenase B Deficiency (C563641)
| ..Lactic Aciduria due to D-Lactic Acid (C565446)
| ..Leukotriene C4 Synthase Deficiency (C565439)
| ..Lipid Metabolism, Inborn Errors (D008052) 135
| ..LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY (OMIM:609016)
| ..Lysosomal Storage Diseases (D016464) 106
| ..Malonic aciduria (C535702)
| ..Mannose 6-Phosphate Receptor Recognition Defect, Lebanese Type (C563601)
| ..Mannose-Binding Protein Deficiency (C563602)
| ..Medium Chain 3-Ketoacyl-CoA Thiolase Deficiency (C566566)
| ..Metal Metabolism, Inborn Errors (D008664) 55
| ..Methemoglobin Reductase Deficiency (C563171)
| ..Methylcobalamin Deficiency, CblG Type (C565394)
| ..Methylmalonyl-Coenzyme A mutase deficiency (C537573)
| ..Mitochondrial Complex II Deficiency (C565375)
| ..Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form, With Methylmalonic Aciduria, Autosomal Recessive (C567624)
| ..Myeloperoxidase Deficiency (C562864)
| ..N acetyltransferase deficiency (C536107)
| ..Pancreatic Insufficiency, Combined Exocrine (C564907)
| ..Peroxisomal Disorders (D018901) 39
| ..Phenacetin O-Deethylase, Deficiency of (C565127)
| ..Phenol sulfotransferase deficiency (C537895)
| ..Phosphoglycerate Kinase 1 Deficiency (C567067)
| ..Porphyrias (D011164) 18
| ..Progeria (D011371) 11
| ..Proguanil, Poor Metabolism of (C563704)
| ..Purine-Pyrimidine Metabolism, Inborn Errors (D011686) 24
| ..Renal Tubular Transport, Inborn Errors (D015499) 76
| ..Retinol-Binding Protein Deficiency (C566711)
| ..Steroid Metabolism, Inborn Errors (D043202) 34
| ..Stomatocytosis I (C566111)
| ..Stomatocytosis II (C566110)
| ..Succinic Acidemia (C563952)
| ..THYROTROPIN-RELEASING HORMONE DEFICIENCY (OMIM:275120)
| ..Transcobalamin I Deficiency (C562798)
| ..Trimethylaminuria (C536561)
| ..Warfarin Sensitivity (C567080)
| ..Weinstein Kliman Scully syndrome (C536688)
| ..Wiedemann Oldigs Oppermann syndrome (C536705)
| ..Xanthinuria, Type I (C562584)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 10688 |
Name: | Stomatocytosis I |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D000137|MESH:D000745|MESH:D008661 |
TreeNumbers: | C15.378.071.141.150/C566111 |C16.320.070/C566111 |C16.320.565/C566111 |C18.452.076/C566111 |C18.452.648/C566111 |
Synonyms: | Overhydrated Hereditary Stomatocytosis |Potassium-Sodium Disorder Of Erythrocyte |
Slim Mappings: | Blood disease|Genetic disease (inborn)|Metabolic disease |
Reference: |
MedGen: C566111
MeSH: C566111
OMIM: 185000;
Genes: STOM; | Phenotypes | | Disease Causing ClinVar Variants | Variation_Name | GeneID | GeneSymbol | ClinicalSignificance | dbSNP | RCVaccession | TestedInGTR | PhenotypeIDs | Chromosome | Start | Stop | HGVS_c | HGVS_p | HGVS_g | OtherIDs | Disease_ClinVar | Disease_hgmd | NM_000324.2(RHAG):c.194T>C (p.Phe65Ser) | 6005 | RHAG | Pathogenic | 863225468 | RCV000202428; | N | MedGen:C1861455,OMIM:185000,ORPHA:3203 | 6 | 49587039 | 49587039 | NM_000324.2:c.194T>C | NP_000315.2:p.Phe65Ser | NC_000006.11:g.49587039A>G | OMIM Allelic Variant:180297.0011 | C1861455 185000 Stomatocytosis I | | | NM_000324.2(RHAG):c.182T>G (p.Ile61Arg) | 6005 | RHAG | Pathogenic | 863225469 | RCV000202426; | N | MedGen:C1861455,OMIM:185000,ORPHA:3203 | 6 | 49587051 | 49587051 | NM_000324.2:c.182T>G | NP_000315.2:p.Ile61Arg | NC_000006.11:g.49587051A>C | OMIM Allelic Variant:180297.0012 | C1861455 185000 Stomatocytosis I | | |
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