Amelogenesis imperfecta

Symptom Information:

Symptom ID: HPO:0000705
Synonyms:
Amelogenesis imperfecta [OMIM:Amelogenesis imperfecta]
Amelogenesis imperfecta (1 patient) [OMIM:Amelogenesis imperfecta (1 patient)]
Amelogenesis imperfecta (in 1 patient) [OMIM:Amelogenesis imperfecta (in 1 patient)]
Amelogenesis imperfecta (secondary teeth) [OMIM:Amelogenesis imperfecta (secondary teeth)]
Quality:
Cross references:
OMIM: "Amelogenesis imperfecta" [OMIM:Amelogenesis imperfecta]
OMIM: "Amelogenesis imperfecta (1 patient)" [OMIM:Amelogenesis imperfecta (1 patient)]
OMIM: "Amelogenesis imperfecta (in 1 patient)" [OMIM:Amelogenesis imperfecta (in 1 patient)]
OMIM: "Amelogenesis imperfecta (secondary teeth)" [OMIM:Amelogenesis imperfecta (secondary teeth)]
Is a (Direct Parents):
HPO         Abnormality of dental enamel
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormality of the mouth(HPO:0000153)
                   Abnormality of the oral cavity(HPO:0000163)
                      Abnormality of the teeth(HPO:0000164)
                         Abnormality of dental structure(HPO:0011061)
                            Abnormality of dental enamel(HPO:0000682)
                               Amelogenesis imperfecta(HPO:0000705)
MedDRA:
Database Frequency: 25 / 7739
Resource:

All diseases associated with this symptom:

AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA2 (OMIM:612529)
AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA3 (OMIM:613211)
AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4 (OMIM:614832)
AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA5 (OMIM:615887)
AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 2 (OMIM:301201)
AMELOGENESIS IMPERFECTA, TYPE IA (OMIM:104530)
AMELOGENESIS IMPERFECTA, TYPE IC (OMIM:204650)
AMELOGENESIS IMPERFECTA, TYPE IE (OMIM:301200)
AMELOGENESIS IMPERFECTA, TYPE IF (OMIM:616270)
AMELOGENESIS IMPERFECTA, TYPE IH (OMIM:616221)
Amelo-cerebro-hypohidrotic syndrome (Orphanet:1946)
Amelogenesis imperfecta - nephrocalcinosis (Orphanet:1031)
Amelogenesis imperfecta and gingival hyperplasia syndrome (Orphanet:171836)
Brachyolmia-amelogenesis imperfecta syndrome (Orphanet:2899)
Deafness - enamel hypoplasia - nail defects (Orphanet:3220)
Hypocalcified amelogenesis imperfecta (Orphanet:100032)
Hypomaturation amelogenesis imperfecta (Orphanet:100033)
Hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism (Orphanet:100034)
Hypoplastic amelogenesis imperfecta (Orphanet:100031)
Jalili syndrome (Orphanet:1873)
LOC syndrome (Orphanet:2407)
NEUROENDOCRINE CARCINOMA OF SALIVARY GLANDS, SENSORINEURAL HEARINGLOSS, AND ENAMEL HYPOPLASIA (OMIM:603641)
RHIZOMELIC DYSPLASIA, SCOLIOSIS, AND RETINITIS PIGMENTOSA (OMIM:610319)
TMEM165-CDG (Orphanet:314667)
Timothy syndrome (Orphanet:65283)