OMOP Concept 4217370
Aase syndrome
StandardConditionSNOMED71988008Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Aase syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 150924 | Aase syndrome | Non-standard |
| MeSH | C538442 | Aase Smith syndrome 2 | Non-standard |
Synonyms
Alternative names recorded for Aase syndrome across source vocabularies.
- Aase Smith II syndrome
- Aase syndrome (disorder)
- anemia de Blackfan-Diamond
- anemia hipoplásica congénita de Blackfan-Diamond
- aplasia pura de serie roja congénita
- Blackfan-Diamond anaemia
- Blackfan-Diamond anemia
- Congenital hypoplastic anaemia Blackfan-Diamond type
- Congenital hypoplastic anemia Blackfan-Diamond type
- Congenital pure red cell aplasia
- síndrome de Aase
- síndrome de Aase Smith II
- síndrome de Aase (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(42)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Congenital hypoplastic anemia
- 1Developmental hereditary disorder
- 1Hereditary cancer-predisposing syndrome
- 1Hereditary disorder of cellular element of blood
- 2Autosomal hereditary disorder
- 2Congenital anemia
- 2Congenital anomaly of the hematopoietic system
- 2Developmental disorder
- 2Disorder of cellular component of blood
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Hypoplastic anemia
- 3Anemia
- 3Anemia due to decreased red cell production
- 3Bone marrow disorder
- 3Congenital disease
- 3Congenital malformation
- 3Disease
- 3Disorder of body system
- 3Disorder of hematopoietic structure
- 3Finding of blood, lymphatics and immune system
- 3Genetic disease
- 3Hemoglobin below reference range
- 3Red blood cell count below reference range
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