dysostosis
bone development disease that results in defective ossification of located in bone
Facts
7 properties- Instance of
- class of disease
- Subclass of
- bone development disease, developmental defect during embryogenesis
- Genetic association
- RAB34, TMEM251, ZRSR2, SCNM1, ALX3, ALX4, BTRC, CDH3, CREBBP, DHODH, DLL3, DLX5, EDNRA, MECOM, EYA1, FGF9, FGFR1, FGFR2, FGFR3, GDF5, GDF6, GLI2, GLI3, HOXA11, HOXA13, IL11RA, LFNG, LMNA, LMX1B, NOG, PAX1, PDE3A, PRKAR1A, RBM8A, SF3B4, SEM1, FBXW4, SHH, SKI, TBX5, TBX6, TCF12, TCOF1, WNT10B, WNT7A, LMBR1, IFT52, SALL4, HES7, TP63, KAT6B, MAP3K20, RNU12, POLR1D, RIPPLY2, TBC1D32, TCTN3, C2CD3, EPS15L1, DDX59, CPLANE1, TMEM107, EOGT, RSPO2, SPECC1L, IFT140, MESP2, EFTUD2[7][8][9][10][11][12][13][14][15][16][17][18][19][20]
- Health specialty
- medical genetics[6]
- ICD-9-CM
- 756.9[4]
- NCI Thesaurus ID
- C34560[5]
- On focus list of Wikimedia project
- WikiProject Medicine
🏷️ Also known as
en dysostosis
ar خلل تكوين العظام
ar سوء التعظم
ar عسر التعظم
ar خلل التعظم
cs dysostóza
de Dysostose
es disostosis
he הפרעה בהתגרמות
he פרע התגרמות
it disostosi
ru дизостоз
🔖 Identifiers · 18
- OpenAlex ID
- C2777203189
- Disease Ontology ID
- DOID:1934
- DiseasesDB
- 31424
- Exact match
- purl.obolibrary.org, identifiers.org, www.orpha.net
- Gran Enciclopèdia Catalana ID
- disostosi
- Gran Enciclopèdia Catalana ID (former scheme)
- 0099448
- MeSH descriptor ID
- D004413
- MeSH tree code
- C05.116.099.370
- Microsoft Academic ID (discontinued)
- 2777203189
- Mondo ID
- MONDO_0018234
- Orphanet ID
- 364559
- Raras disease ID
- D364559
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