Prominent glabella
Symptom Information:
Symptom ID: | HPO:0002057 | ||
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 forehead(HPO:0000290) Abnormality of the glabella(HPO:0002056) Prominent glabella(HPO:0002057) MedDRA: |
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Database Frequency: | 8 / 7739 | ||
Resource: |
All diseases associated with this symptom:
8q22.1 microdeletion syndrome | (Orphanet:178303) |
Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome | (Orphanet:306542) |
MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE | (OMIM:300861) |
Microcephaly - deafness - intellectual deficit | (Orphanet:2533) |
Pitt-Hopkins-like syndrome 2 | (OMIM:614325) |
Prominent glabella - microcephaly - hypogenitalism | (Orphanet:2083) |
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY | (OMIM:614800) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |