Amelogenesis imperfecta, hypomaturation-hypoplasia type
Symptom Information:
Symptom ID:
|
OMIM : No Id available
|
Synonyms:
|
|
Quality:
|
|
Cross references:
|
OMIM: "Amelogenesis imperfecta, hypomaturation-hypoplasia type" [OMIM:Amelogenesis imperfecta, hypomaturation-hypoplasia type] |
|
Is a (Direct Parents):
|
|
Is a (Whole tree):
|
HPO:
MedDRA:
|
Database Frequency:
|
1 / 7739
|
Resource:
|
|
All diseases associated with this symptom:
Hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism
|
(Orphanet:100034)
|