Abnormality of dental color
Symptom Information:
Symptom ID: | HPO:0011073 | ||||||||||||||||||||||||||||||||||||||
Synonyms: |
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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 color(HPO:0011073) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Dental and gingival conditions(MedDRA:10044018) Dental surface disorders(MedDRA:10012329) Abnormality of dental color(HPO:0011073) |
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Database Frequency: | 24 / 7739 | ||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AMELOGENESIS IMPERFECTA, TYPE IE | (OMIM:301200) |
AMELOGENESIS IMPERFECTA, TYPE IF | (OMIM:616270) |
Acro-oto-ocular syndrome | (Orphanet:2980) |
Alopecia antibody deficiency | (Orphanet:1006) |
Alström syndrome | (Orphanet:64) |
Amelo-cerebro-hypohidrotic syndrome | (Orphanet:1946) |
Amelo-onycho-hypohidrotic syndrome | (Orphanet:1028) |
Amelogenesis imperfecta - nephrocalcinosis | (Orphanet:1031) |
Amelogenesis imperfecta and gingival hyperplasia syndrome | (Orphanet:171836) |
Congenital erythropoietic porphyria | (Orphanet:79277) |
Ehlers-Danlos syndrome, dermatosparaxis type | (Orphanet:1901) |
Hereditary sensory and autonomic neuropathy type 4 | (Orphanet:642) |
Jalili syndrome | (Orphanet:1873) |
Keratosis follicularis spinulosa decalvans | (Orphanet:2340) |
Linear nevus sebaceus syndrome | (Orphanet:2612) |
Metaphyseal dysplasia - maxillary hypoplasia - brachydacty | (Orphanet:2504) |
Osteogenesis imperfecta | (Orphanet:666) |
Pierre Robin syndrome - faciodigital anomaly | (Orphanet:2888) |
Pontocerebellar hypoplasia, type 9 | (OMIM:615809) |
Stoll-Alembik-Finck syndrome | (Orphanet:3200) |
Timothy syndrome | (Orphanet:65283) |
Tricho-dento-osseous syndrome | (Orphanet:3352) |
Usher syndrome | (Orphanet:886) |
Usher syndrome type 2 | (Orphanet:231178) |