Underdeveloped supraorbital ridges

Symptom Information:

Symptom ID: HPO:0009891
Synonyms:
Depressed supraorbital ridge [HPO:0009891]
Flat supraorbital ridge [HPO:0009891]
Hypoplasia of the supraorbital ridges [HPO:0009891]
Hypoplastic supraorbital ridge [HPO:0009891]
Hypoplastic supraorbital ridges [HPO:0009891]
Shallow orbital ridges [HPO:0009891]
Shallow supraorbital ridge [HPO:0009891]
Underdeveloped brows [HPO:0009891]
Depressed supraorbital ridge [OMIM:Depressed supraorbital ridge]
Flat supraorbital ridge [OMIM:Flat supraorbital ridge]
Hypoplastic supraorbital ridge [OMIM:Hypoplastic supraorbital ridge]
Hypoplastic supraorbital ridges [OMIM:Hypoplastic supraorbital ridges]
Shallow orbital ridges [OMIM:Shallow orbital ridges]
Shallow supraorbital ridge [OMIM:Shallow supraorbital ridge]
Flat supraorbital ridge [Orphanet:3420]
Flat supraorbital ridges [OMIM:Flat supraorbital ridges]
Quality:
Cross references:
HPO:0000586 "Shallow orbits" [Orphanet:3420]
Orphanet:3420 "Flat supraorbital ridge" [Orphanet:3420]
OMIM: "Depressed supraorbital ridge" [OMIM:Depressed supraorbital ridge]
OMIM: "Flat supraorbital ridge" [OMIM:Flat supraorbital ridge]
OMIM: "Hypoplastic supraorbital ridge" [OMIM:Hypoplastic supraorbital ridge]
OMIM: "Hypoplastic supraorbital ridges" [OMIM:Hypoplastic supraorbital ridges]
OMIM: "Shallow orbital ridges" [OMIM:Shallow orbital ridges]
OMIM: "Shallow supraorbital ridge" [OMIM:Shallow supraorbital ridge]
OMIM: "Flat supraorbital ridges" [OMIM:Flat supraorbital ridges]
Is a (Direct Parents):
HPO         Abnormality of the supraorbital ridges
Orphanet Abnormal facial shape
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:
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)