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158 Possible Causes for Congenital Stationary Night Blindness Type 2A

  • Familial Hypercholesterolemia

    Blindness, Congenital Stationary, Type 1D 4 Night Blindness, Congenital Stationary, Type 1E 2 Night Blindness, Congenital Stationary, Type 1F 3 Night Blindness, Congenital[preventiongenetics.com] Stationary, Type 1G 2 Night Blindness, Congenital Stationary, Type 2A 4 Night Blindness, Congenital Stationary, Type 2B 6 Nijmegen Breakage Syndrome 8 Nijmegen Breakage Syndrome-Like[preventiongenetics.com] Rhodopsin-Related 4 Night Blindness, Congenital Stationary, Type 1A 3 Night Blindness, Congenital Stationary, Type 1B 2 Night Blindness, Congenital Stationary, Type 1C 2 Night[preventiongenetics.com]

  • Dilated Cardiomyopathy Type 2B

    Blindness, Congenital Stationary, Type 1D 4 Night Blindness, Congenital Stationary, Type 1E 2 Night Blindness, Congenital Stationary, Type 1F 3 Night Blindness, Congenital[preventiongenetics.com] Stationary, Type 1G 2 Night Blindness, Congenital Stationary, Type 2A 4 Night Blindness, Congenital Stationary, Type 2B 6 Nijmegen Breakage Syndrome 8 Nijmegen Breakage Syndrome-Like[preventiongenetics.com] Rhodopsin-Related 4 Night Blindness, Congenital Stationary, Type 1A 3 Night Blindness, Congenital Stationary, Type 1B 2 Night Blindness, Congenital Stationary, Type 1C 2 Night[preventiongenetics.com]

  • Congenitally Short Costocoracoid Ligament

    Anemia Congenital stationary night blindness, type 1A Congenital stationary night blindness, type 2A Congenital Stenosis of Cervical Medullary Canal Congenital Stromal Corneal[diseaseinfosearch.org] Congenital secretory diarrhea, sodium type Congenital sensory neuropathy with selective loss of small myelinated fibers Congenital Short Femur Congenital Spherocytic Hemolytic[diseaseinfosearch.org] […] dislocation (CPD) Congenital phenobarbital exposure Congenital Porphyria Congenital Pseudoarthrosis Congenital radio-ulnar synostosis Congenital secretory diarrhea, chloride type[diseaseinfosearch.org]

  • Hereditary Hyperekplexia

    Neuropathy, congenital hypomyelinating, autosomal dominant Congenital stationary night blindness, type 2B VACTERL association with hydrocephaly, X-linked Congenital stationary[amp.pharm.mssm.edu] night blindness, type 2A Mental retardation, X-linked, syndromic 32 Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type Microcephaly[amp.pharm.mssm.edu] Congenital diaphragmatic hernia (CDH) and/or omphalocele are common (see these terms).[amp.pharm.mssm.edu]

  • Autosomal Dominant Congenital Stationary Night Blindness Type 2

    blindness type 1 congenital stationary Night blindness Type 1A Congenital Stationary Night Blindness Type 1B Congenital Stationary Night Blindness Type 2 Congenital Stationary[lsd-project.jp] Genetics Congenital stationary night blindness type 2A is an X-linked disorder caused by a mutation in the CACNA1F gene located at Xp11.23.[disorders.eyes.arizona.edu] […] nonprogressive CACNA1F Aland Island eye disease; Cone-rod dystrophy, X-linked, 3; Night blindness, congenital stationary (incomplete), 2A, X-linked CHM Choroideremia GNAT1[asperbio.com]

  • Laron Syndrome with Immunodeficiency

    blindness 1 0 Night blindness, congenital stationary, autosomal dominant 2; CSNBAD2 Congenital stationary night blindness 1 0 Night blindness, congenital stationary, type[guidetopharmacology.org] Blindness, Congenital Stationary, Type 1D 6 Night Blindness, Congenital Stationary, Type 1E 3 Night Blindness, Congenital Stationary, Type 1F 4 Night Blindness, Congenital[preventiongenetics.com] 2A ; CSNB2A Congenital stationary night blindness 1 0 Night blindness, congenital stationary, type 1B; CSNB1B Congenital stationary night blindness 1 0 Night blindness, congenital[guidetopharmacology.org]

  • Autosomal Recessive Spastic Paraplegia Type 55

    VI GHR OMIM CA2 Autosomal recessive osteopetrosis 3 X-linked incomplete congenital stationary night blindness 2A OMIM CAPN3 Limb-girdle muscular dystrophy, type 2A GHR GeneReviews[genepeeks.com] […] deficiency GHR GeneReviews OMIM BUB1B Mosaic variegated aneuploidy syndrome 1 Spastic paraplegia 55 GHR GeneReviews OMIM C2ORF71 Retinitis pigmentosa 54 Orofaciodigital syndrome, type[genepeeks.com]

  • Gingival Fibromatosis-Progressive Deafness Syndrome

    Blindness, Congenital Stationary, Type 1D 4 Night Blindness, Congenital Stationary, Type 1E 2 Night Blindness, Congenital Stationary, Type 1F 3 Night Blindness, Congenital[preventiongenetics.com] Stationary, Type 1G 2 Night Blindness, Congenital Stationary, Type 2A 4 Night Blindness, Congenital Stationary, Type 2B 6 Nijmegen Breakage Syndrome 8 Nijmegen Breakage Syndrome-Like[preventiongenetics.com] Rhodopsin-Related 4 Night Blindness, Congenital Stationary, Type 1A 3 Night Blindness, Congenital Stationary, Type 1B 2 Night Blindness, Congenital Stationary, Type 1C 2 Night[preventiongenetics.com]

  • Night Blindness

    blindness type 1 congenital stationary Night blindness Type 1A Congenital Stationary Night Blindness Type 1B Congenital Stationary Night Blindness Type 2 Congenital Stationary[lsd-project.jp] Genetics Congenital stationary night blindness type 2A is an X-linked disorder caused by a mutation in the CACNA1F gene located at Xp11.23.[disorders.eyes.arizona.edu] Night Blindness Type 2A Congenital Stationary Night Blindness Type 2B Congenital Stationary Night Blindness X-Linked Complete CSNB X-linked congenital stationary night blindness[lsd-project.jp]

  • Combined Oxidative Phosphorylation Defect Type 14

    Blindness, Congenital Stationary, Type 1D 4 Night Blindness, Congenital Stationary, Type 1E 2 Night Blindness, Congenital Stationary, Type 1F 3 Night Blindness, Congenital[preventiongenetics.com] Stationary, Type 1G 2 Night Blindness, Congenital Stationary, Type 2A 4 Night Blindness, Congenital Stationary, Type 2B 6 Nijmegen Breakage Syndrome 8 Nijmegen Breakage Syndrome-Like[preventiongenetics.com] Rhodopsin-Related 4 Night Blindness, Congenital Stationary, Type 1A 3 Night Blindness, Congenital Stationary, Type 1B 2 Night Blindness, Congenital Stationary, Type 1C 2 Night[preventiongenetics.com]

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