Preferred Name |
Facial Hemihypertrophy |
|
Synonyms |
Hemifacial Hyperplasia |
|
ID |
http://purl.bioontology.org/ontology/MESH/C563014 |
|
altLabel |
Hemifacial Hyperplasia |
|
cui |
C1399354 |
|
Has mapping qualifier | ||
HM |
D006965 D005146/Q000151 D005145/Q000002 |
|
Inverse of RB |
0 |
|
Mapped to |
http://purl.bioontology.org/ontology/MESH/D006965 |
|
MDA |
20121105 |
|
MeSH Frequency |
65 |
|
MMR |
20150818 |
|
notation |
C563014 |
|
prefLabel |
Facial Hemihypertrophy |
|
SC |
3 |
|
Scope Statement |
A congenital autosomal dominant abnormality characterized by asymmetry of the MANDIBLE, hypoplasia of the MAXILLA, and dental MALOCCLUSION. OMIM: 133900 |
|
TERMUI |
T802004 T802005 |
|
TH |
OMIM (2013) |
|
tui |
T047 |
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