Broad alveolar ridges
Symptom Information:
Symptom ID: | HPO:0000187 | |||||||
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 alveolar ridges(HPO:0006477) Broad alveolar ridges(HPO:0000187) MedDRA: |
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Database Frequency: | 14 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
Bohring-Opitz syndrome | (Orphanet:97297) |
CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE | (OMIM:218400) |
HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVEFACIAL FEATURES | (OMIM:609943) |
Intellectual disability-developmental delay-contractures syndrome | (Orphanet:3454) |
Malignant hyperthermia - arthrogryposis - torticollis | (Orphanet:2215) |
Micrencephaly - corpus callosum agenesis - abnormal genitalia | (Orphanet:2508) |
Mucolipidosis type 2 | (Orphanet:576) |
OCULODENTODIGITAL DYSPLASIA | (OMIM:164200) |
Oculodentodigital dysplasia | (Orphanet:2710) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
Perlman syndrome | (Orphanet:2849) |
Short stature - wormian bones - dextrocardia | (Orphanet:2863) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Taurodontia - absent teeth - sparse hair | (Orphanet:2731) |