AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 2

General Information (adopted from Orphanet):

Synonyms, Signs: AMELOGENESIS IMPERFECTA 3, HYPOPLASTIC TYPE, FORMERLY
ENAMEL HYPOPLASIA, X-LINKED
AIH3, FORMERLY
Number of Symptoms 3
OrphanetNr:
OMIM Id: 301201
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: X-linked inheritance
[Omim]
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
(HPO:0000705) Amelogenesis imperfecta 25 / 7739
2
(HPO:0001417) X-linked inheritance 173 / 7739
3
(OMIM) Amelogenesis imperfecta, hypoplastic 5 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: