short rib dysplasia
human disease
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short rib dysplasia
Summary
short rib dysplasia is a developmental defect during embryogenesis[1].
Key Facts
- short rib dysplasia's instance of is recorded as developmental defect during embryogenesis[2].
- short rib dysplasia's instance of is recorded as rare disease[3].
- short rib dysplasia's instance of is recorded as class of disease[4].
- short rib dysplasia's subclass of is recorded as primary bone dysplasia[5].
- short rib dysplasia's OMIM ID is recorded as 617405[6].
- short rib dysplasia's KEGG ID is recorded as H02157[7].
- short rib dysplasia's Orphanet ID is recorded as 93426[8].
- short rib dysplasia's ICD-9-CM is recorded as 756.3[9].
- short rib dysplasia's genetic association is recorded as DYNLT2B[10].
- short rib dysplasia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_93426[11].
- short rib dysplasia's UMLS CUI is recorded as C0432195[12].
- short rib dysplasia's ICD-10-CM is recorded as Q77.2[13].
- short rib dysplasia's Mondo ID is recorded as MONDO_0019691[14].
- short rib dysplasia's ICD-11 ID is recorded as LD24.B[15].
- short rib dysplasia's ICD-11 ID is recorded as 399834960[16].