Dentin Dysplasia Gene, QTL, and Strain Annotations - Disease Ontology

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Keyword

ONTOLOGY REPORT

Dentin Dysplasia (D003805)

An apparently hereditary disorder of dentin formation, marked by a normal appearance of coronal dentin associated with pulpal obliteration, faulty root formation, and a tendency for peripheral lesions without obvious cause. (From Dorland, 27th ed)

There are 3 path(s) and 4 annotation(s) to this term. Annotations to this term and its descendants total 4.

ANNOTATIONS

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Dentin Dysplasia

Gene Symbol	Gene Name	Evidence	Reference
ACLY	ATP citrate lyase	ISS	RGD:1300342
Acly	ATP citrate lyase	ISS	RGD:1300342
DSPP	dentin sialophosphoprotein	ISS	RGD:734904
Dspp	dentin sialophosphoprotein	ISS	RGD:734904

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in the second column. The C column indicates the number of objects annotated to the term, while the T column indicates the number of annotations to the term and its decendants.

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Term	C	T
Disease Ontology	0	8271
Stomatognathic Diseases	0	62
Tooth Diseases	0	18
Tooth Abnormalities	0	12
Dentin Dysplasia	4	4
Go to path: [ 1 ][ 2 ][ 3 ][ back to top ]
Term	C	T
Disease Ontology	0	8271
Stomatognathic Diseases	0	62
Stomatognathic System Abnormalities	0	21
Tooth Abnormalities	0	12
Dentin Dysplasia	4	4
Go to path: [ 1 ][ 2 ][ 3 ][ back to top ]
Term	C	T
Disease Ontology	0	8271
Congenital, Hereditary, and Neonatal Diseases and Abnormalities	3	1039
Abnormalities	0	456
Stomatognathic System Abnormalities	0	21
Tooth Abnormalities	0	12
Dentin Dysplasia	4	4

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