| Descriptor English: | Osteopetrosis | ||||||
| Descriptor Spanish: |
Osteopetrosis
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| Descriptor Portuguese: | Osteopetrose | ||||||
| Descriptor French: | Ostéopétrose | ||||||
| Entry term(s): |
Albers Schoenberg Disease Albers Schonberg Disease Albers Schonberg Disease, Autosomal Dominant Albers Schönberg Disease Albers-Schoenberg Disease Albers-Schonberg Disease Albers-Schonberg Disease, Autosomal Dominant Albers-Schönberg Disease Autosomal Dominant Osteopetrosis Type 2 Congenital Osteopetrosis Disease, Albers-Schoenberg Disease, Albers-Schonberg Disease, Albers-Schönberg Disease, Marble Bone Marble Bone Disease Marble Bones, Autosomal Dominant Osteopetroses Osteopetrosis Autosomal Dominant Type 2 Osteopetrosis, Autosomal Dominant 2 Osteopetrosis, Autosomal Dominant, Type II Osteosclerosis Fragilis Osteosclerosis Fragilis Generalisata Osteosclerosis Fragilis Generalisatas |
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| Tree number(s): |
C05.116.099.708.702.678 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D010022 | ||||||
| Scope note: | Excessive formation of dense trabecular bone leading to pathological fractures; OSTEITIS; SPLENOMEGALY with infarct; ANEMIA; and extramedullary hemopoiesis (HEMATOPOIESIS, EXTRAMEDULLARY). |
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| Annotation: | do not confuse with OSTEOPOROSIS |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| DeCS ID: | 10203 | ||||||
| Unique ID: | D010022 | ||||||
| NLM Classification: | WE 250 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1966/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2013/07/08 |
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Osteopetrosis
- Preferred
Osteopetrosis Autosomal Dominant Type 2
- Narrower
Congenital Osteopetrosis
- Narrower
| Concept UI |
M0015549 |
| Scope note | Excessive formation of dense trabecular bone leading to pathological fractures; OSTEITIS; SPLENOMEGALY with infarct; ANEMIA; and extramedullary hemopoiesis (HEMATOPOIESIS, EXTRAMEDULLARY). |
| Preferred term | Osteopetrosis |
| Entry term(s) |
Albers Schoenberg Disease Albers Schonberg Disease Albers Schönberg Disease Albers-Schoenberg Disease Albers-Schonberg Disease Albers-Schönberg Disease Disease, Albers-Schoenberg Disease, Albers-Schonberg Disease, Albers-Schönberg Disease, Marble Bone Marble Bone Disease Osteopetroses Osteosclerosis Fragilis Osteosclerosis Fragilis Generalisata Osteosclerosis Fragilis Generalisatas |
| Concept UI |
M0531502 |
| Preferred term | Osteopetrosis Autosomal Dominant Type 2 |
| Entry term(s) |
Albers Schonberg Disease, Autosomal Dominant Albers-Schonberg Disease, Autosomal Dominant Autosomal Dominant Osteopetrosis Type 2 Marble Bones, Autosomal Dominant Osteopetrosis, Autosomal Dominant 2 Osteopetrosis, Autosomal Dominant, Type II |
| Concept UI |
M0583797 |
| Preferred term | Congenital Osteopetrosis |
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