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Summary Literature (0)
DOID:0110087 - asphyxiating thoracic dystrophy 3

Disease Ontology Definition:An asphyxiating thoracic dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the DYNC2H1 gene on chromosome 11q22.

Synonyms: ATD3, SRPS1, SRPS2B, SRPS3, SRTD3, Saldino-Noonan syndrome, Verma-Naumoff syndrome, polydactyly with neonatal chondrodystrophy, type I, polydactyly with neonatal chondrodystrophy, type III, short rib-polydactyly syndrome, type I, short rib-polydactyly syndrome, type IIB, short-rib thoracic dysplasia 3 with or without polydactyly,

Xenbase Genes : dync2h1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013127 - asphyxiating thoracic dystrophy 3


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): asphyxiating thoracic dystrophy (is_a), autosomal recessive disease (is_a)