Hyperplasia of midface
Symptom Information:
Symptom ID: | HPO:0012371 | ||||||
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 midface(HPO:0000309) Hyperplasia of midface(HPO:0012371) MedDRA: |
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Database Frequency: | 10 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Aicardi syndrome | (Orphanet:50) |
Autosomal recessive spastic paraplegia type 20 | (Orphanet:101000) |
Beta-thalassemia major | (Orphanet:231214) |
Dislocation of the hip - dysmorphism | (Orphanet:2412) |
Ehlers-Danlos syndrome, classic type | (Orphanet:287) |
Microcephaly - cervical spine fusion anomalies | (Orphanet:2522) |
Oculo-reno-cerebellar syndrome | (Orphanet:2715) |
POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY | (OMIM:611087) |
Paraplegia - intellectual deficit - hyperkeratosis | (Orphanet:2824) |
Tricho-dento-osseous syndrome | (Orphanet:3352) |