Create issue ticket

58 Possible Causes for Hyperbiliverdinemia, Loss of Vision

  • 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] He showed mental retardation and visual impairment in the first decade which gradually developed along with motor dysfunction for over 40 years.[ncbi.nlm.nih.gov] The onset of sleep disturbance was associated with the onset of both seizures (ρ 0.5834, P 0.0001) and loss of vision (ρ 0.3840, P 0.0084).[ncbi.nlm.nih.gov]

  • 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] , [44] pituitary hormone deficiencies [45] Eye Loss of vision, [42] proptosis [46] Cardiovascular Constrictive pericarditis, [47] heart block, [27] ruptured aortic aneurysm[infogalactic.com] , [9] pituitary hormone deficiencies [10] Eye Loss of vision, [7] proptosis [11] Cardiovascular Constrictive pericarditis , [12] heart block , [13] ruptured aortic aneurysm[howlingpixel.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] impairment-urinary anomalies syndrome Hypotonia-speech impairment-severe cognitive delay syndrome Hypotrichosis-intellectual disability, Lopes type Hypoxanthine guanine phosphoribosyltransferase[se-atlas.de] […] skin Granulosa cell cancer Granulosa cell malignant tumor Gravidic intrahepatic cholestasis Gray platelet syndrome Grayson-Wilbrandt corneal dystrophy Greenberg dysplasia Green[orpha.net]

  • 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] Major symptoms include vertigo and vision loss 6.[quizlet.com] impairment Cleft palate Motor delay Abnormality of the cerebral ventricles Small cell lung carcinoma Gray matter heterotopias Sacrococcygeal teratoma Expressive language[mendelian.co]

  • Hereditary Hyperekplexia

    Joubert syndrome 17 Cardiac conduction defect, nonspecific Lethal multiple pterygium syndrome Non-small cell lung cancer Acroerythrokeratoderma Renal hypodysplasia/aplasia 2 Hyperbiliverdinemia[amp.pharm.mssm.edu] Norrie Disease Norrie disease (ND) is a very rare X-linked genetic disorder which primarily causes blindness or significant vision loss in boys from birth.[geneticdisordersuk.org] impairment.[amp.pharm.mssm.edu]

  • Craniodiaphyseal Dysplasia

    Joubert syndrome 17 Cardiac conduction defect, nonspecific Lethal multiple pterygium syndrome Non-small cell lung cancer Acroerythrokeratoderma Renal hypodysplasia/aplasia 2 Hyperbiliverdinemia[amp.pharm.mssm.edu] ) blindness Impaired hearing (progressive) deafness Other ocular problems Strabismus Bulging eyes (exophthalmos) Loss of binocular vision Hypertelorism Seizures Mental retardation[healthh.com] […] of vision [ 4 ] Deformation of ossicles due to bony overgrowth Significant brain compression Epilepsy Complete hearing inability Reduced air spaces of mastoid, middle ear[primehealthchannel.com]

  • 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] impairment-urinary anomalies Intellectual deficit - sparse hair - brachydactyly Isolated anophthalmia - microphthalmia Juvenile Huntington disease LIG4 syndrome Li-Fraumeni[csbg.cnb.csic.es] 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]

  • Familial Benign Flecked Retina

    jaundice Green monkey disease Greig cephalopolysyndactyly syndrome Greither disease GRFoma GRF tumor Grisart-Destrée syndrome Griscelli-Pruniéras syndrome Griscelli-Pruniéras[orpha.net] This leads to rapid death of retinal cells, thereby resulting in severe loss of vision.[codelay.com] Presentation - there is progressive visual loss in the third decade, particularly peripheral and night vision.[patient.info]

  • Hereditary Hyperphosphatasia

    Hyperandrogenism Due to Cortisone Reductase Deficiency HYP625 Hyperbilirubinemia, Rotor Type HYP236 HBLRR Hyperbilirubinemia, Transient Familial Neonatal HYP766 HBLRTFN Hyperbiliverdinemia[malacards.org] The alterations in the skull can lead to teeth loss and the compression of the optical nerve cause loss of vision.[flipper.diff.org] impairment Skin abnormalities (ichthyosis, etc.)[igd.biken.osaka-u.ac.jp]

  • Waters-West Syndrome

    21-hydroxylase deficiency, 201910 UGT1A1 Hyperbilirubinemia, familial transcient neonatal, 237900 SLCO1B1- SLCO1B3 Hyperbilirubinemia, Rotor type, digenic, 237450 BLVRA Hyperbiliverdinemia[gsdseq.ir] Learn more about how to achieve it with Mendelian Learn more Other signs and symptoms that you may find interesting Visual impairment and Low-set, posteriorly rotated ears[mendelian.co] impairment Autosomal dominant inheritance Hypoplasia of the corpus callosum Cleft palate Autosomal recessive inheritance Pica Hearing impairment Feeding difficulties Low-set[mendelian.co]

Further symptoms

Similar symptoms