Abnormality of the forehead
Symptom Information:
| Symptom ID: | HPO:0000290 | ||||
| Synonyms: |
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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 forehead(HPO:0000290) MedDRA: |
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| Database Frequency: | 5 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| Arterial calcification, generalized, of infancy, 1 | (OMIM:208000) |
| ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMALDOMINANT | (OMIM:614940) |
| ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMALRECESSIVE | (OMIM:614941) |
| Fabry disease | (Orphanet:324) |
| Pontocerebellar hypoplasia, type 9 | (OMIM:615809) |