Underdeveloped supraorbital ridges
Symptom Information:
Symptom ID: | HPO:0009891 | ||||||||||||||||
Synonyms: |
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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 orbital region(HPO:0000315) Abnormality of the supraorbital ridges(HPO:0100538) Underdeveloped supraorbital ridges(HPO:0009891) MedDRA: |
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Database Frequency: | 36 / 7739 | ||||||||||||||||
Resource: |
All diseases associated with this symptom:
3MC SYNDROME 1 | (OMIM:257920) |
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 | (Orphanet:98791) |
Aminopterin/methotrexate embryofetopathy | (Orphanet:1908) |
Antley-Bixler syndrome | (Orphanet:83) |
Bohring-Opitz syndrome | (Orphanet:97297) |
CARDIOFACIOCUTANEOUS SYNDROME 1 | (OMIM:115150) |
Camptodactyly syndrome, Guadalajara type 1 | (Orphanet:1327) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Carpenter syndrome | (Orphanet:65759) |
Cerebro-oculo-nasal syndrome | (Orphanet:66625) |
Combined immunodeficiency with facio-oculo-skeletal anomalies | (Orphanet:221139) |
Craniofacial dyssynostosis | (Orphanet:1516) |
Craniosynostosis, Boston type | (Orphanet:1541) |
Dubowitz syndrome | (Orphanet:235) |
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3C | (OMIM:609384) |
FRONTOOCULAR SYNDROME | (OMIM:605321) |
GAPO syndrome | (Orphanet:2067) |
Gorlin-Chaudhry-Moss syndrome | (Orphanet:2095) |
Isolated brachycephaly | (Orphanet:35099) |
Jackson-Weiss syndrome | (Orphanet:1540) |
Laron syndrome | (Orphanet:633) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 27 | (OMIM:615866) |
Megalocornea-intellectual deficit syndrome | (Orphanet:2479) |
Microbrachycephaly - ptosis - cleft lip | (Orphanet:2511) |
Microcephaly - lymphedema - chorioretinopathy | (Orphanet:2526) |
Mullerian derivatives - lymphangiectasia - polydactyly | (Orphanet:1655) |
Pierre Robin syndrome - faciodigital anomaly | (Orphanet:2888) |
Pseudoaminopterin syndrome | (Orphanet:221120) |
Roberts syndrome | (Orphanet:3103) |
Syndromic diarrhea | (Orphanet:84064) |
TARP syndrome | (Orphanet:2886) |
TRICHOHEPATOENTERIC SYNDROME 1 | (OMIM:222470) |
Tetralogy of Fallot | (Orphanet:3303) |
Trigonocephaly - broad thumbs | (Orphanet:3365) |
Trisomy 18 | (Orphanet:3380) |
Zellweger syndrome | (Orphanet:912) |