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68 Possible Causes for Hyperbiliverdinemia, Retinitis Pigmentosa

  • 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] Weleber, Retinitis Pigmentosa and Allied Disorders, Retina, 10.1016/B978-1-4557-0737-9.00040-0, (761-835), (2013).[doi.org] Neuro-ophthalmological abnormalities like optic atrophy (50%), macular degeneration (33.3%) and retinitis pigmentosa (8.3%) were seen in two thirds.[ncbi.nlm.nih.gov]

  • 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] retinitis pigmentosa with PRPH2 RP1 Dominant retinitis pigmentosa RP1L1 Occult macular dystrophy, Retinitis pigmentosa RP2 X-linked retinitis pigmentosa RP9 dominant retinitis[molecularvisionlab.com] Retinitis pigmentosa RP1L1 Occult macular dystrophy, Retinitis pigmentosa RP2 Retinitis pigmentosa RPE65 Leber congenital amaurosis, Retinitis pigmentosa RPGR Retinitis pigmentosa[genda.com.ar]

  • 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] 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] pigmentosa-foveoschisis-optic disc drusen syndrome 4 Cases 727 Microscopic polyangiitis 1.0 I * 83463 Microtia 15.5 BP 139450 Microtia-eye coloboma- imperforation of the[azkurs.org]

  • Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome

    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] pigmentosa Retinitis pigmentosa 10 Retinitis Pigmentosa 11 Retinitis pigmentosa 12 Retinitis Pigmentosa 13 Retinitis Pigmentosa 14 Retinitis Pigmentosa 15 Retinitis Pigmentosa[pentacorelab.hu] Pigmentosa retinitis pigmentosa & Leber congenital amaurosis; Joubert syndrome, Meckel syndrome Retinitis pigmentosa 25 (RP25) Retinitis pigmentosa 26 (RP26) Retinitis pigmentosa[babygene.co.il]

  • Hypergonadotropic Hypogonadism-Cataract Syndrome

    Hyperbilirubinemia, Rotor Type; HBLRR OMIM:237800 Hyperbilirubinemia, Shunt, Primary; PSHB OMIM:237900 Hyperbilirubinemia, Transient Familial Neonatal; HBLRTFN OMIM:614156 Hyperbiliverdinemia[informatics.jax.org] Learn more Other less relevant matches: Low match RETINITIS PIGMENTOSA Retinitis pigmentosa (RP) is an inherited retinal dystrophy leading to progressive loss of the photoreceptors[mendelian.co] pigmentosa-1) RP2 (Retinitis pigmentosa-2) RP9 (Retinitis pigmentosa-9) RPE65 (Leber congenital amaurosis 2) RPGR (Cone-rod dystrophy-1) RPGRIP1 (Cone-rod dystrophy 13) RPGRIP1L[en.praenatal-medizin.de]

  • Waters-West Syndrome

    21-hydroxylase deficiency, 201910 UGT1A1 Hyperbilirubinemia, familial transcient neonatal, 237900 SLCO1B1- SLCO1B3 Hyperbilirubinemia, Rotor type, digenic, 237450 BLVRA Hyperbiliverdinemia[gsdseq.ir] Retinitis Pigmentosa 5 Retinitis Pigmentosa 1 5 Retinitis Pigmentosa 10 4 Retinitis Pigmentosa 11 4 Retinitis Pigmentosa 12 5 Retinitis Pigmentosa 13 5 Retinitis Pigmentosa[preventiongenetics.com] ) Retinitis pigmentosa-18 ( HPRP3) Retinitis pigmentosa-19 ( ABCA4) Retinitis pigmentosa-2 ( RP2) Retinitis pigmentosa-25 ( EYS) Retinitis pigmentosa-26 ( CERKL) Retinitis[en.praenatal-medizin.de]

  • 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] Retinitis Pigmentosa 5 Retinitis Pigmentosa 1 5 Retinitis Pigmentosa 10 4 Retinitis Pigmentosa 11 4 Retinitis Pigmentosa 12 5 Retinitis Pigmentosa 13 5 Retinitis Pigmentosa[preventiongenetics.com] A new case of Zimmermann–Laband syndrome with atypical retinitis pigmentosa. Acta Derm Venereol 1992; 72 ( 5): 376–379. 16. Shah N, Gupta YK, Ghose S.[nature.com]

  • Hereditary Hypercarotenemia and Vitamin A Deficiency

    Hyperbilirubinemia, Rotor Type; HBLRR OMIM:237800 Hyperbilirubinemia, Shunt, Primary; PSHB OMIM:237900 Hyperbilirubinemia, Transient Familial Neonatal; HBLRTFN OMIM:614156 Hyperbiliverdinemia[informatics.jax.org] pigmentosa-1) RP2 (Retinitis pigmentosa-2) RP9 (Retinitis pigmentosa-9) RPE65 (Leber congenital amaurosis 2) RPGR (Cone-rod dystrophy-1) RPGRIP1 (Cone-rod dystrophy 13) RPGRIP1L[en.praenatal-medizin.de] 21-hydroxylase deficiency, 201910 UGT1A1 Hyperbilirubinemia, familial transcient neonatal, 237900 SLCO1B1- SLCO1B3 Hyperbilirubinemia, Rotor type, digenic, 237450 BLVRA Hyperbiliverdinemia[gsdseq.ir]

  • 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] pigmentosa-1) RP2 (Retinitis pigmentosa-2) RP9 (Retinitis pigmentosa-9) RPE65 (Leber congenital amaurosis 2) RPGR (Cone-rod dystrophy-1) RPGRIP1 (Cone-rod dystrophy 13) RPGRIP1L[en.praenatal-medizin.de] […] gene - - 7.2 RP2 Retinitis Pigmentosa Deletion and duplication analysis; Sequencing of all coding exons of the gene - - 1.1 RPE65 Autosomal Dominant Retinitis Pigmentosa Sequencing[cegat.de]

  • Nestor-Guillermo Progeria Syndrome

    Maturity onset diabetes of the young, type 11, BLM Bloom syndrome, BLNK Agammaglobulinemia 4, BLOC1S3 Hermansky Pudlak syndrome 8, BLOC1S6 Hermansky pudlak syndrome 9, BLVRA Hyperbiliverdinemia[healthdocbox.com] Disease Type of connection Familial isolated dilated cardiomyopathy X-linked Emery-Dreifuss muscular dystrophy Cone rod dystrophy Leber congenital amaurosis Retinitis pigmentosa[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]

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