OMOP Concept 4034963
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness
StandardConditionSNOMED237617006Disorder
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 Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C536510 | Thiamine responsive megaloblastic anemia syndrome | Non-standard |
| Nebraska Lexicon | 237617006 | Thiamine-responsive megaloblastic anaemia syndrome | Non-standard |
Synonyms
Alternative names recorded for Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness across source vocabularies.
- anemia megaloblástica sensible a tiamina, con diabetes mellitus y sordera neurosensorial
- anemia megaloblástica sensible a tiamina, con diabetes mellitus y sordera neurosensorial (trastorno)
- anemia megaloblástica sensible a tiamina, con diabetes mellitus y sordera sensorioneural
- Megaloblastic anaemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness
- Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness (disorder)
- Rogers syndrome
- síndrome de anemia megaloblástica sensible a tiamina
- síndrome de Rogers
- Thiamine-responsive megaloblastic anaemia syndrome
- Thiamine-responsive megaloblastic anemia syndrome
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(85)Roll up to these when you need a wider cohort.
- 1Auditory system hereditary disorder
- 1Autosomal recessive hereditary disorder
- 1Congenital anomaly of endocrine gland
- 1Congenital malformation of pancreas
- 1Congenital sensorineural hearing loss
- 1Decreased hearing
- 1Developmental hereditary disorder
- 1Diabetes mellitus associated with genetic syndrome
- 1Digestive system hereditary disorder
- 1Disorder of endocrine pancreas
- 1Hereditary disorder of cellular element of blood
- 1Hereditary disorder of endocrine system
- 1Thiamine-responsive megaloblastic anemia
- 2Autosomal hereditary disorder
- 2Congenital anomaly of abdomen
- 2Congenital anomaly of digestive organ
- 2Congenital hearing disorder
- 2Congenital malformation
- 2Decline in functional status
- 2Developmental disorder
- 2Disorder of auditory system
- 2Disorder of cellular component of blood
- 2Disorder of digestive system
- 2Disorder of endocrine system
- 2Disorder of pancreas
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