Broad face
Symptom Information:
Symptom ID: | HPO:0000283 | ||||
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) Abnormal facial shape(HPO:0001999) Broad face(HPO:0000283) MedDRA: |
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Database Frequency: | 12 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
2q37 microdeletion syndrome | (Orphanet:1001) |
Aspartylglucosaminuria | (Orphanet:93) |
CHROMOSOME 1p32-p31 DELETION SYNDROME | (OMIM:613735) |
HOLOPROSENCEPHALY 7 | (OMIM:610828) |
Intellectual deficit, X-linked, Nascimento type | (Orphanet:163956) |
Otopalatodigital syndrome | (Orphanet:669) |
PLANTAR LIPOMATOSIS, UNUSUAL FACIES, AND DEVELOPMENTAL DELAY | (OMIM:602342) |
RIENHOFF SYNDROME | (OMIM:615582) |
Recombinant 8 syndrome | (Orphanet:96167) |
Scheie syndrome | (Orphanet:93474) |
Smith-Magenis syndrome | (Orphanet:819) |
Spondylocarpotarsal synostosis | (Orphanet:3275) |