Amelogenesis imperfecta
Symptom Information:
Symptom ID: | HPO:0000705 | ||||
Synonyms: |
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Quality: | |||||
Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |