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89 Possible Causes for Hereditary Areflexic Dystasia

  • Hereditary Areflexic Dystasia

    hereditary areflexic dystasia Roussy-Lйvy hereditary areflexic dystasia Roussy-Lйvy syndrome. Medical dictionary. 2011.[medicine.academic.ru] Name Roussy-Levy Hereditary Areflexic Dystasia Synonyms ROUSSY-LEVY SYNDROME Classification genetic, neurological Phenotypes Abnormality of the immune system ; Areflexia ;[mousephenotype.org] HEREDITARY AREFLEXIC DYSTASIA Roussy-Levy Syndrome Roussy-Lévy syndrome edit English Roussy–Lévy syndrome human disease Hereditary areflexic dystasia, Roussy-LC)vy type Hereditary[wikidata.org]

  • Retinohepatoendocrinologic Syndrome

    areflexic dystasia Rowley-Rosenberg syndrome Roy Maroteaux Kremp syndrome Rozin Hertz Goodman syndrome Rubella virus antenatal infection Rubinstein Taybi like syndrome Rubinstein-Taybi[mindmappedia.com] areflexic dystasia Rowley-Rosenberg syndrome Roy Maroteaux Kremp syndrome Rozin Hertz Goodman syndrome Rubella virus antenatal infection Rubella, congenital Rubella Rubinstein[fact-index.com] areflexic dystasia Rowley-Rosenberg syndrome Roy Maroteaux Kremp syndrome Rozin Hertz Goodman syndrome Ru Rubella virus antenatal infection Rubella, congenital Rubella Rubeola[ssf.f15ijp.com]

  • Hereditary Motor and Sensory Neuropathy

    The ICD code G600 is used to code Roussy-Lévy syndrome Roussy-Lévy syndrome, also known as Roussy-Lévy hereditary areflexic dystasia, is a rare genetic disorder of humans[icd.codes] Areflexic Dystasia Roussy-Levy Syndrome 180800 Genetic Test Registry Scapuloperoneal Spinal Muscular Atrophy Amyotrophy, Neurogenic Scapuloperoneal, New England Type SPSMA[ukgtn.nhs.uk] Rhizomelic Chondrodysplasia Punctata, Type 1 Chondrodysplasia Punctata, Rhizomelic Form Chondrodystrophia Calcificans Punctata RCDP1 CDPR 215100 Genetic Test Registry Roussy-Levy Hereditary[ukgtn.nhs.uk]

  • Tarsal Tunnel Syndrome

    areflexic dystasia; Charcot–Marie–Tooth (CMT) disease type II essential tremor, sensory ataxia, poor coordination and judgement of movement, kyphoscoliosis and distal muscle[medical-dictionary.thefreedictionary.com] […] also characterized by orthostatic hypotension, hyperhidrosis and hyporeflexic/absent deep tendon reflexes, pes cavus and trophic plantar ulceration Roussy–Levy syndrome; hereditary[medical-dictionary.thefreedictionary.com]

  • Renoprival Hypertension

    areflexic dystasia Rowley–Rosenberg syndrome Roy–Maroteaux–Kremp syndrome Rozin–Hertz–Goodman syndrome Ru [ edit ] Rubella virus antenatal infection Rubella, congenital Rubella[en.wikipedia.org] Rommen–Mueller–Sybert syndrome Rosai–Dorfman disease Rosenberg–Chutorian syndrome Rosenberg–Lohr syndrome Roseola infantum Rothmund–Thomson syndrome Rotor syndrome Roussy–Levy hereditary[en.wikipedia.org]

  • Charcot-Marie-Tooth Disease Type 2S

    Areflexic Dystasia Roussy-Levy Syndrome 180800 Genetic Test Registry Spinal Muscular Atrophy, Distal, Autosomal Recessive, 1 I Neuronopathy, Distal Hereditary Motor, Type[ukgtn.nhs.uk] , AUTOSOMAL RECESSIVE ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA Barreto LC, Oliveira FS, Nunes PS, de França Costa IM, Garcez CA, Goes GM, Neves EL, de Souza Siqueira Quintans[ghr.nlm.nih.gov] Neuropathy Hypomyelination, Severe Congenital Neuropathy, Congenital Hypomyelinating, Autosomal Dominant, included CHN CHN CMT4E 605253 Genetic Test Registry Roussy-Levy Hereditary[ukgtn.nhs.uk]

  • Reflex Sympathetic Dystrophy

    areflexic dystasia; Charcot–Marie–Tooth (CMT) disease type II essential tremor, sensory ataxia, poor coordination and judgement of movement, kyphoscoliosis and distal muscle[medical-dictionary.thefreedictionary.com] […] also characterized by orthostatic hypotension, hyperhidrosis and hyporeflexic/absent deep tendon reflexes, pes cavus and trophic plantar ulceration Roussy–Levy syndrome; hereditary[medical-dictionary.thefreedictionary.com]

  • Infantile Choroidocerebral Calcification Syndrome

    Hereditary Motor Sensory Neuropathy. Hereditary Areflexic Dystasia. Rubinstein-Taybi syndrome. Broad thumb-hallux syndrome. Russell-Silver Syndrome (RSS).[neurometplus.com]

  • Complex Regional Pain Syndrome Type II

    areflexic dystasia; Charcot–Marie–Tooth (CMT) disease type II essential tremor, sensory ataxia, poor coordination and judgement of movement, kyphoscoliosis and distal muscle[medical-dictionary.thefreedictionary.com] […] also characterized by orthostatic hypotension, hyperhidrosis and hyporeflexic/absent deep tendon reflexes, pes cavus and trophic plantar ulceration Roussy–Levy syndrome; hereditary[medical-dictionary.thefreedictionary.com]

  • Salti-Salem Syndrome

    […] deficiency type I Hereditary areflexic dystasia - See Roussy Levy syndrome Hereditary ataxia Hereditary ATTR amyloidosis - See Familial transthyretin amyloidosis Hereditary[herenciageneticayenfermedad.blogspot.com] […] antithrombin deficiency Hereditary antithrombin deficiency type 1 - See Hereditary antithrombin deficiency type I Hereditary antithrombin deficiency type 2 Hereditary antithrombin[herenciageneticayenfermedad.blogspot.com] […] type 1 - See Hereditary angioedema Hereditary angioneurotic edema - See Hereditary angioedema Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome Hereditary[herenciageneticayenfermedad.blogspot.com]

Further symptoms