Search Ontology:
Human Disease
asphyxiating thoracic dystrophy 3
- Term ID
- DOID:0110087
- Synonyms
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- ATD3
- polydactyly with neonatal chondrodystrophy, type I
- polydactyly with neonatal chondrodystrophy, type III
- Saldino-Noonan syndrome
- short rib-polydactyly syndrome, type I
- short rib-polydactyly syndrome, type IIB
- short-rib thoracic dysplasia 3 with or without polydactyly
- SRPS1
- SRPS2B
- SRPS3
- SRTD3
- Verma-Naumoff syndrome
- Definition
- An asphyxiating thoracic dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the DYNC2H1 gene on chromosome 11q22. https://www.ncbi.nlm.nih.gov/pubmed/19442771
- References
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- ICD10CM:Q77.2
- MIM:613091
- Ontology
- Human Disease ( DOID:0110087 )
- is a type of
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Genes Involved
Zebrafish Models