OMOP Concept 37116389
Pseudoprogeria syndrome
StandardConditionSNOMED733086003Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Pseudoprogeria syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C563111 | Absent Eyebrows and Eyelashes with Mental Retardation | Non-standard |
Synonyms
Alternative names recorded for Pseudoprogeria syndrome across source vocabularies.
- Absent eyebrows and eyelashes with intellectual disability syndrome
- Hall Berg Rudolph syndrome
- Pseudoprogeria syndrome (disorder)
- síndrome de ausencia de cejas y pestañas con discapacidad intelectual
- síndrome de Hall-Berg-Rudolph
- síndrome de pseudoprogeria
- síndrome de pseudoprogeria (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(103)Roll up to these when you need a wider cohort.
- 1Abnormal nervous system function
- 1Absent eyebrow
- 1Aplasia of skin
- 1Autosomal recessive hereditary disorder
- 1Congenital absence of eyelash
- 1Congenital anomaly of central nervous system
- 1Congenital glaucoma
- 1Congenital microcephaly
- 1Developmental hereditary disorder
- 1Disorder of hair growth
- 1Genetic intellectual disability
- 1Hereditary disorder of the visual system
- 1Inherited metabolic disorder of nervous system
- 1Multiple malformation syndrome with facial defects as major feature
- 1Premature aging syndrome
- 1Tetraplegia
- 2Autosomal hereditary disorder
- 2Complete bilateral paralysis
- 2Congenital alopecia
- 2Congenital anomaly of face
- 2Congenital anomaly of head
- 2Congenital anomaly of nervous system
- 2Congenital disease
- 2Congenital malformation of the eyebrow
- 2Developmental disorder
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