AMELOGENESIS IMPERFECTA, TYPE IF

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 5
OrphanetNr:
OMIM Id: 616270
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
(HPO:0011073) Abnormality of dental color 24 / 7739
2
(HPO:0006297) Hypoplasia of dental enamel 64 / 7739
3
(HPO:0000705) Amelogenesis imperfecta 25 / 7739
4
(HPO:0009722) Dental enamel pits 5 / 7739
5
(HPO:0000007) Autosomal recessive inheritance 2538 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: