Radial Graph - 214800 - CHARGE SYNDROME - OMIM
214800: CHARGE SYNDROME

Graphical representation of phenotype/gene relationship(s) associated with this entry. Phenotypic Series (when available) are displayed with the relevant genes and subsequent phenotypes to a depth of 4 nodes. A quick reference overview and guide (PDF). No hierarchy is implied.   Feedback  

Key:
   ⬤ Phenotype
   ⬤ Gene
   ⬤ Phenotypic series (PS)
• Click circles to show/hide
    downstream relationships.
• Click MIM number or PS
    number to recenter map.
• Click phenotype name or gene
    symbol to go to the MIM entry.
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NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.
OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2024 Johns Hopkins University.

NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.
OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2024 Johns Hopkins University.
Printed: Nov. 5, 2024