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68 Possible Causes for Gaucher Disease, Hyperbiliverdinemia

  • Neuronal Ceroid Lipofuscinosis

    […] dystrophy type III Granular-lattice corneal dystrophy Granulomatosis with polyangiitis Gravidic intrahepatic cholestasis Gray platelet syndrome Gräsbeck-Imerslund disease Green[csbg.cnb.csic.es] […] syndrome and late manifesting forms of several other lysosomal storage disorders (GM2 gangliosidosis, Gaucher disease and Niemann-Pick type C disease; see these terms).[orpha.net] Gaucher disease type I accounts for more than 90% of cases of Gaucher disease ( 40, 41 ).[ncbi.nlm.nih.gov]

  • Glycogen Storage Disease due to Muscle Beta-Enolase Deficiency

    jaundice Green monkey disease Greig cephalopolysyndactyly syndrome Greither disease GRFoma GRF tumor Grisart-Destrée syndrome Griscelli-Pruniéras syndrome Griscelli-Pruniéras[orpha.net] disease 1.0 P * 355 Gaucher disease 1.3 BP 355 Gaucher disease 1.7 I * 77259 Gaucher disease type 1 1.0 P * 77260 Gaucher disease type 2 0.01 P * 77261 Gaucher disease type[azkurs.org] […] that are treated in this facility: Alpha-mannosidosis Argininemia Beta-mannosidosis Citrullinemia Fabry disease GM1 gangliosidosis GM2 gangliosidosis Galactosemia Gaucher[se-atlas.de]

  • Hereditary North American Indian Childhood Cirrhosis

    Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 Hepatoportal sclerosis Hereditary North American Indian childhood cirrhosis Hereditary fructose intolerance Hyperbiliverdinemia[se-atlas.de] , erythropoietic porphyria Gilbert syndrome, Wilson disease, Dubin-Johnson syndrome α 1 -Antitrypsin deficiency, Wilson disease, lipoatrophic diabetes Adults Gaucher disease[clinicalgate.com] .  α1-antitrypsin deficiency  Cystic fibrosis  Fructosemia  Galactosemia  Gaucher’s disease  Glycogen storage disease, type III  Glycogen storage disease, type IV 17[slideshare.net]

  • Waters-West Syndrome

    21-hydroxylase deficiency, 201910 UGT1A1 Hyperbilirubinemia, familial transcient neonatal, 237900 SLCO1B1- SLCO1B3 Hyperbilirubinemia, Rotor type, digenic, 237450 BLVRA Hyperbiliverdinemia[gsdseq.ir] […] syndrome 2 612736 GBA 1q22 Gaucher disease, perinatal lethal 608013 Gaucher disease, type I 230800 Gaucher disease, type II 230900 Gaucher disease, type III 231000 Gaucher[institutobernabeu.com] 17-alpha-hydroxylase deficiency Gaucher disease type 3 Orstavik Lindemann Solberg syndrome Cronkhite-Canada disease Spinocerebellar ataxia with dysmorphism Ectropion inferior[checkrare.com]

  • Familial Recurrent Peripheral Facial Palsy

    jaundice Green monkey disease Greig cephalopolysyndactyly syndrome Greither disease GRFoma GRF tumor Grisart-Destrée syndrome Griscelli-Pruniéras syndrome Griscelli-Pruniéras[orpha.net] disease type 2 Gaucher disease type 3 Generalized bulbospinal muscular atrophy Generalized epilepsy with febrile seizures-plus Generalized epilepsy-paroxysmal dyskinesia[se-atlas.de] disease Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome Gaucher disease, subacute neuronopathic type Gaucher disease type 1 Gaucher disease type 2 Gaucher[orpha.net]

  • Autosomal Recessive Primary Microcephaly Type 10

    […] to 21-hydroxylase deficiency, 201910 UGT1A1 Hyperbilirubinemia, familial transcient neonatal, 237900 SLCO1B1-SLCO1B3 Hyperbilirubinemia, Rotor type, digenic, 237450 BLVRA Hyperbiliverdinemia[gsdseq.ir] Disease Gaucher Disease , Perinatal Lethal Glutamine Deficiency, Congenital GM1-Gangliosidosis , Type II Goldberg-Shprintzen Megacolon Syndrome Goldenhar Syndrome Hemorrhagic[familydiagnosis.com] Hyperbiliverdinemia, 614156 (3) BLVRB G:600941 . . BLZF1 G:608692 . . BMF G:606266 . . BMI1 G:164831 . . BMIQ1 P:606641 . . BMIQ2 P:606643 . . BMIQ3 P:607446 . .[usegalaxy.org]

  • Transient Familial Neonatal Hyperbilirubinemia

    Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 Hepatoportal sclerosis Hereditary North American Indian childhood cirrhosis Hereditary fructose intolerance Hyperbiliverdinemia[se-atlas.de] disease 骨粗鬆症 osteoporosis 骨軟化症 osteomalasia コプロポルフィリン症 coproporphyria コリー病 コーリ病,糖原病III型 Cori disease, glycogen storage disease (type III) コルセット肝 corset liver[jsge.or.jp] […] hemolytic anemias (hereditary spherocytosis, thalassemia, hemoglobinopathies), storage disorders (Gaucher’s disease, Niemann-Pick disease), mucopolysaccharide disorders ([ccfpprep.com]

  • Gingival Fibromatosis-Progressive Deafness Syndrome

    jaundice Green monkey disease Greig cephalopolysyndactyly syndrome Greither disease GRFoma GRF tumor Grisart-Destrée syndrome Griscelli-Pruniéras syndrome Griscelli-Pruniéras[orpha.net] 17-alpha-hydroxylase deficiency Gaucher disease type 3 Orstavik Lindemann Solberg syndrome Cronkhite-Canada disease Spinocerebellar ataxia with dysmorphism Ectropion inferior[checkrare.com] Disease, Atypical, Due To Saposin C Deficiency 1 Gaucher Disease, Perinatal Lethal 2 Gaucher Disease, Type 1 1 Gaucher Disease, Type II 1 Gaucher Disease, Type III 1 Gaucher[preventiongenetics.com]

  • IgG4-Related Hepatopathy

    Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 Hepatoportal sclerosis Hereditary North American Indian childhood cirrhosis Hereditary fructose intolerance Hyperbiliverdinemia[se-atlas.de] disease 骨粗鬆症 osteoporosis 骨軟化症 osteomalasia コプロポルフィリン症 coproporphyria コリー病 コーリ病,糖原病III型 Cori disease, glycogen storage disease (type III) コルセット肝 corset liver[jsge.or.jp] […] hypothyroidism 甲状腺中毒症 thyrotoxicosis 後天性免疫不全症候群 acquired immune deficiency syndrome 高コレステロール血症 hypercholesterolemia 高トリグリセリド血症 hypertriglyceridemia 高リポ蛋白血症 hyperlipoproteinemia ゴーシェ病 Gaucher[jsge.or.jp]

  • Hereditary Hyperphosphatasia

    Hyperandrogenism Due to Cortisone Reductase Deficiency HYP625 Hyperbilirubinemia, Rotor Type HYP236 HBLRR Hyperbilirubinemia, Transient Familial Neonatal HYP766 HBLRTFN Hyperbiliverdinemia[malacards.org] Gaucher’s disease ( Fig. 14.25a, b ) Lower extremities are involved more often.[musculoskeletalkey.com] disease.[genecards.org]

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