204099004: Agenesis of eye (disorder)
Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Expanded Value Set
Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Congenital aphakia |
Is a |
False |
Agenesis of eye |
Inferred relationship |
Some |
|
Congenital cystic eyeball (disorder) |
Is a |
False |
Agenesis of eye |
Inferred relationship |
Some |
|
Congenital aniridia (disorder) |
Is a |
False |
Agenesis of eye |
Inferred relationship |
Some |
|
Anophthalmos |
Is a |
False |
Agenesis of eye |
Inferred relationship |
Some |
|
Monophthalmos |
Is a |
False |
Agenesis of eye |
Inferred relationship |
Some |
|
A very rare multiple congenital anomaly syndrome characterized by the presence of anophthalmia or severe microphthalmia, cleft lip/palate, facial cleft and sacral neural tube defects, along with various additional anomalies including congenital glaucoma, iris coloboma, primary hyperplastic vitreous, hypertelorism, low-set ears, clinodactyly, choanal atresia/stenosis, dysgenesis of sacrum, tethering of spinal cord, syringomyelia, hypoplasia of corpus callosum, cerebral ventriculomegaly and endocrine abnormalities. An autosomal recessive inheritance has been suggested. |
Is a |
False |
Agenesis of eye |
Inferred relationship |
Some |
|
Reference Sets
Concept inactivation indicator reference set
Description inactivation indicator reference set
GB English
US English
SAME AS association reference set (foundation metadata concept)
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