Broad alveolar ridges

Symptom Information:

Symptom ID: HPO:0000187
Synonyms:
Broad alveolar margins [HPO:0000187]
Widened alveolar ridges [HPO:0000187]
Alveolar ridge overgrowth [Orphanet:10700]
Broad alveolar margins [OMIM:Broad alveolar margins]
Broad alveolar ridges [OMIM:Broad alveolar ridges]
Widened alveolar ridges [OMIM:Widened alveolar ridges]
Broad alveolar ridge [Orphanet:10700]
Quality:
Cross references:
HPO:0009085 "Alveolar ridge overgrowth" [Orphanet:10700]
Orphanet:10700 "Broad alveolar ridge" [Orphanet:10700]
OMIM: "Broad alveolar margins" [OMIM:Broad alveolar margins]
OMIM: "Broad alveolar ridges" [OMIM:Broad alveolar ridges]
OMIM: "Widened alveolar ridges" [OMIM:Widened alveolar ridges]
Is a (Direct Parents):
Orphanet Abnormality of the tongue
HPO         Abnormality of the alveolar ridges
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:
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)