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bn:21538650n
Noun Named Entity
Categories: Genetic disorders with no OMIM, Rare diseases, Genetic disorders
EN
SADDAN  Severe achondroplasia with developmental delay and acanthosis nigricans  ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS  ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN  SADDAN dysplasia
EN
SADDAN is a rare inherited disorder of bone growth characterized by skeletal, brain, and skin abnormalities. Wikipedia
Definitions
Relations
Sources
EN
SADDAN is a rare inherited disorder of bone growth characterized by skeletal, brain, and skin abnormalities. Wikipedia
Severe achondroplasia with developmental delay and acanthosis nigricans is a very rare genetic disorder. Wikipedia
Autosomal dominant disease characterized by severe achondroplasia, developmental delay and acanthosis nigricans that has material basis in heterozygous mutation in the FGFR3 gene on chromosome 4p16 Wikidata
IS A
rare disease
achondroplasia
GENETIC ASSOCIATION
fibroblast growth factor receptor 3
Wikipedia
EN
SADDAN, Severe achondroplasia with developmental delay and acanthosis nigricans
Wikidata
EN
SADDAN
Wikipedia Redirections
EN
SADDAN, Severe Achondroplasia with Developmental Delay and Acanthosis Nigricans
Wikidata Alias
EN
ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS, ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN, SADDAN, SADDAN dysplasia, severe achondroplasia with developmental delay and acanthosis nigricans, Severe Achondroplasia with Developmental Delay and Acanthosis Nigricans

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