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Metadata
ID DOID:0111158
Name SADDAN
Definition A syndrome characterized by severe achondroplasia, developmental delay and acanthosis nigricans that has_material_basis_in heterozygous mutation in the FGFR3 gene on chromosome 4p16.
https://ghr.nlm.nih.gov/condition/saddan, https://www.ncbi.nlm.nih.gov/pubmed/10053006
Xrefs

GARD:9443

MESH:D000130

OMIM:616482

ORDO:85165

SNOMEDCT_US_2023_03_01:699870002

UMLS_CUI:C2674173

Subsets

DO_rare_slim

Synonyms

SADDAN dysplasia [EXACT]

severe achondroplasia with developmental delay and acanthosis nigricans [EXACT]

Parent Relationships

is_a syndrome

is_a autosomal dominant disease

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