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Hypoplastic amelogenesis imperfecta
4 OMIM references -
2 associated genes
16 connected diseases
No signs/symptoms info
Disease Type of connection
Generalized junctional epidermolysis bullosa, non-Herlitz type
Junctional epidermolysis bullosa, Herlitz type
Acral dystrophic epidermolysis bullosa
Centripetalis recessive dystrophic epidermolysis bullosa
Dystrophic epidermolysis bullosa pruriginosa
Dystrophic epidermolysis bullosa, nails only
Epidermolysis bullosa simplex superficialis
Generalized dominant dystrophic epidermolysis bullosa
Pretibial dystrophic epidermolysis bullosa
Recessive dystrophic epidermolysis bullosa inversa
Recessive dystrophic epidermolysis bullosa-generalized other
Severe generalized recessive dystrophic epidermolysis bullosa
Transient bullous dermolysis of the newborn
LOC syndrome
Osteogenesis imperfecta type 3
Junctional epidermolysis bullosa inversa
Synonym(s):
- Amelogenesis imperfecta type 1
Classification (Orphanet):
- Rare genetic disease
- Rare odontologic disease
Classification (ICD10):
- Diseases of the digestive system -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
4 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
ENAM Q9NRM1606585
LAMB3 Q13751150310
No signs/symptoms info available.