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Diseases

Amelogenesis Imperfecta, Type Ib

amelogenesis imperfecta, type ib

Entity Type
Diseases
Relation Groups
1
Relation Preview
8

Basic Information

Grouped by core information, identifiers, and descriptions.

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Core Information

Disease Name
Amelogenesis Imperfecta, Type Ib
Standard Disease Name
amelogenesis imperfecta, type ib
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
C537270
OMIM ID
229120
UMLS ID
C0795944
HPO ID
No data

Description and Extensions

Description
JABL99:Coarse facies, mental retardation, hearing loss, and skeletal abnormalities are the major symptoms.
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
03
CYP1A2
cytochrome P450 family 1 subfamily A member 2
cytochrome P450 family 1 subfamily A member 2
04
CYP2D6
cytochrome P450 family 2 subfamily D member 6
cytochrome P450 family 2 subfamily D member 6