78642008: Ocular albinism, type I (disorder)
- SNOMED CT Concept\Clinical finding\...
- \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Albinism\Ocular albinism\Ocular albinism, type I
- \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the visual system\Ocular albinism\Ocular albinism, type I
- \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Albinism\Ocular albinism\Ocular albinism, type I
- \Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\X-linked recessive hereditary disease\Ocular albinism, type I
- \Disease\Disorder of pigmentation\Albinism\Ocular albinism\Ocular albinism, type I
- \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the visual system\Ocular albinism\Ocular albinism, type I
- \Disease\Disorder of body system\Visual system disorder\Disorder of eye region\Disorder of eye\Anomaly of eye\Lesion of eye\Ocular albinism\Ocular albinism, type I
- \Disease\Disorder of body system\Visual system disorder\Disorder of eye region\Disorder of eye\Anomaly of eye\Congenital anomaly of eye\Ocular albinism\Ocular albinism, type I
- \Disease\Disorder of body system\Visual system disorder\Hereditary disorder of the visual system\Ocular albinism\Ocular albinism, type I
- \Disease\Disorder of body system\Visual system disorder\Congenital anomaly of visual system\Congenital anomaly of eye\Ocular albinism\Ocular albinism, type I
- \Disease\Disorder of head\Disorder of eye region\Disorder of eye\Anomaly of eye\Lesion of eye\Ocular albinism\Ocular albinism, type I
- \Disease\Disorder of head\Disorder of eye region\Disorder of eye\Anomaly of eye\Congenital anomaly of eye\Ocular albinism\Ocular albinism, type I
- \Disease\Disorder of head\Congenital anomaly of head\Congenital anomaly of eye\Ocular albinism\Ocular albinism, type I
- \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Albinism\Ocular albinism\Ocular albinism, type I
- \Disease\Congenital disease\Congenital anomaly\Congenital anomaly of visual system\Congenital anomaly of eye\Ocular albinism\Ocular albinism, type I
- \Disease\Congenital disease\Congenital anomaly\Congenital anomaly of head\Congenital anomaly of eye\Ocular albinism\Ocular albinism, type I
- \Disease\Congenital disease\Congenital anomaly\Albinism\Ocular albinism\Ocular albinism, type I
- \Disease\Congenital disease\Inborn error of metabolism\Albinism\Ocular albinism\Ocular albinism, type I
- \Disease\Developmental disorder\Developmental hereditary disorder\Albinism\Ocular albinism\Ocular albinism, type I
- \Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of visual system\Congenital anomaly of eye\Ocular albinism\Ocular albinism, type I
- \Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of head\Congenital anomaly of eye\Ocular albinism\Ocular albinism, type I
- \Disease\Developmental disorder\Congenital anomaly\Albinism\Ocular albinism\Ocular albinism, type I
Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Expanded Value Set
Outbound Relationships |
Type |
Target |
Active |
Characteristic |
Refinability |
Group |
Values |
Ocular albinism, type I |
Pathological process |
Pathological developmental process |
true |
Inferred relationship |
Some |
1 |
|
Ocular albinism, type I |
Occurrence |
Congenital |
true |
Inferred relationship |
Some |
1 |
|
Ocular albinism, type I |
Is a |
X-linked recessive hereditary disease |
true |
Inferred relationship |
Some |
|
|
Ocular albinism, type I |
Associated morphology |
Congenital hypopigmentation |
false |
Inferred relationship |
Some |
1 |
|
Ocular albinism, type I |
Associated morphology |
Decreased melanin pigmentation |
false |
Inferred relationship |
Some |
1 |
|
Ocular albinism, type I |
Is a |
X-linked hereditary disease |
false |
Inferred relationship |
Some |
|
|
Ocular albinism, type I |
Is a |
Ocular albinism |
true |
Inferred relationship |
Some |
|
|
Ocular albinism, type I |
Finding site |
Eye structure |
true |
Inferred relationship |
Some |
1 |
|
Ocular albinism, type I |
Associated morphology |
Decreased melanin pigmentation |
true |
Inferred relationship |
Some |
1 |
|
Ocular albinism, type I |
Associated morphology |
Congenital hypopigmentation |
false |
Inferred relationship |
Some |
1 |
|
Ocular albinism, type I |
Occurrence |
Congenital |
false |
Inferred relationship |
Some |
2 |
|
Ocular albinism, type I |
Occurrence |
Congenital |
false |
Inferred relationship |
Some |
3 |
|
Ocular albinism, type I |
Associated morphology |
Decreased melanin pigmentation |
false |
Inferred relationship |
Some |
2 |
|
Ocular albinism, type I |
Associated morphology |
Congenital hypopigmentation |
false |
Inferred relationship |
Some |
3 |
|
Ocular albinism, type I |
Finding site |
Skin structure |
false |
Inferred relationship |
Some |
3 |
|
Ocular albinism, type I |
Finding site |
Orbital region structure |
false |
Inferred relationship |
Some |
1 |
|
Ocular albinism, type I |
Finding site |
Structure of skin region |
false |
Inferred relationship |
Some |
2 |
|
Ocular albinism, type I |
Associated morphology |
Congenital anomaly |
false |
Inferred relationship |
Some |
1 |
|
Ocular albinism, type I |
Finding site |
Structure of nervous system |
false |
Inferred relationship |
Some |
|
|
Ocular albinism, type I |
Finding site |
Eye structure |
false |
Inferred relationship |
Some |
1 |
|
Ocular albinism, type I |
Associated morphology |
Congenital hypopigmentation |
false |
Inferred relationship |
Some |
1 |
|
Ocular albinism, type I |
Associated morphology |
Congenital deficiency |
false |
Inferred relationship |
Some |
|
|
Ocular albinism, type I |
Occurrence |
Congenital |
false |
Inferred relationship |
Some |
|
|
Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set
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