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76 Possible Causes for Onset between 15 and 27 Years, Persistent Notochordal Canal

  • Anxiety Disorder

    […] of the age-of-onset distributions) of only 8 years (age 7-15 years) for impulse-control disorders, 9 years (age 18-27 years) for substance use disorders, and 15 years (age[doi.org] Second, age of onset was concentrated in a very narrow age range for most disorders, with interquartile ranges (IQRs) (ie, the number of years between the 25th and 75th percentiles[doi.org]

    Missing: Persistent Notochordal Canal
  • Mental Disorder

    […] of the age-of-onset distributions) of only 8 years (age 7-15 years) for impulse-control disorders, 9 years (age 18-27 years) for substance use disorders, and 15 years (age[doi.org] Second, age of onset was concentrated in a very narrow age range for most disorders, with interquartile ranges (IQRs) (ie, the number of years between the 25th and 75th percentiles[doi.org]

    Missing: Persistent Notochordal Canal
  • Familial Recurrent Peripheral Facial Palsy

    notochordal canal syndrome Salla disease Salt-and-pepper syndrome Sandhoff disease Sandhoff disease, adult form Sandhoff disease, infantile form Sandhoff disease, juvenile[se-atlas.de] […] syndrome SLC35A1-CDG SLC35A2-CDG SSR4-CDG STT3A-CDG STT3B-CDG SURF1-related Charcot-Marie-Tooth disease type 4 Sacral agenesis-abnormal ossification of the vertebral bodies-persistent[se-atlas.de]

    Missing: Onset between 15 and 27 Years
  • Chronic Anxiety

    […] of the age-of-onset distributions) of only 8 years (age 7-15 years) for impulse-control disorders, 9 years (age 18-27 years) for substance use disorders, and 15 years (age[dx.doi.org] Second, age of onset was concentrated in a very narrow age range for most disorders, with interquartile ranges (IQRs) (ie, the number of years between the 25th and 75th percentiles[dx.doi.org]

    Missing: Persistent Notochordal Canal
  • Infantile-Onset Ascending Hereditary Spastic Paralysis

    notochordal canal syndrome Salla disease Salt-and-pepper syndrome Sandhoff disease Sandhoff disease, adult form Sandhoff disease, infantile form Sandhoff disease, juvenile[se-atlas.de] […] syndrome SLC35A1-CDG SLC35A2-CDG SSR4-CDG STT3A-CDG STT3B-CDG SURF1-related Charcot-Marie-Tooth disease type 4 Sacral agenesis-abnormal ossification of the vertebral bodies-persistent[se-atlas.de]

    Missing: Onset between 15 and 27 Years
  • Distal Hereditary Motor Neuropathy Type 1

    notochordal canal syndrome Salla disease Salt-and-pepper syndrome Sandhoff disease Sandhoff disease, adult form Sandhoff disease, infantile form Sandhoff disease, juvenile[se-atlas.de] […] syndrome SLC35A1-CDG SLC35A2-CDG SSR4-CDG STT3A-CDG STT3B-CDG SURF1-related Charcot-Marie-Tooth disease type 4 Sacral agenesis-abnormal ossification of the vertebral bodies-persistent[se-atlas.de]

    Missing: Onset between 15 and 27 Years
  • Retinal Degeneration-Nanophthalmos-Glaucoma Syndrome

    notochordal canal syndrome 4 Cases 794 Saethre-Chotzen syndrome 3.0 BP * 300493 Sagliker syndrome 60 Cases 140969 Saldino-Mainzer syndrome 10 Cases 370938 Salt-and-pepper[azkurs.org] Rotor syndrome 50 Cases 83616 Rubella panencephalitis 20 Cases 783 Rubinstein-Taybi syndrome 0.7 BP * 397927 Sacral agenesis-abnormal ossification of the vertebral bodies-persistent[azkurs.org]

    Missing: Onset between 15 and 27 Years
  • Anxiety Neurosis

    […] of the age-of-onset distributions) of only 8 years (age 7-15 years) for impulse-control disorders, 9 years (age 18-27 years) for substance use disorders, and 15 years (age[doi.org] Second, age of onset was concentrated in a very narrow age range for most disorders, with interquartile ranges (IQRs) (ie, the number of years between the 25th and 75th percentiles[doi.org]

    Missing: Persistent Notochordal Canal
  • Limb-Girdle Muscular Dystrophy Type 2J

    notochordal canal syndrome Salla disease Salt-and-pepper syndrome Sandhoff disease Sandhoff disease, adult form Sandhoff disease, infantile form Sandhoff disease, juvenile[se-atlas.de] […] syndrome SLC35A1-CDG SLC35A2-CDG SSR4-CDG STT3A-CDG STT3B-CDG SURF1-related Charcot-Marie-Tooth disease type 4 Sacral agenesis-abnormal ossification of the vertebral bodies-persistent[se-atlas.de]

    Missing: Onset between 15 and 27 Years
  • Meningomyelocele

    […] splits around that adhesion or persistence of the neurenteric canal, which would leave a connection of pluripotent cells between the ectoderm and the endoderm. [8] The role[asianjns.org] […] theories postulated are neoplastic transformation of misplaced primordial germ cells from the yolk sac, an ectodermal-to-endodermal adhesion forms during gastrulation and the notochord[asianjns.org]

    Missing: Onset between 15 and 27 Years

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