Absent frontal sinuses

Symptom Information:

Symptom ID: HPO:0002688
Synonyms:
Absence of frontal sinuses [HPO:0002688]
Absent frontal sinus [HPO:0002688]
Frontal sinus agenesis [Orphanet:8660]
Absence of frontal sinuses [OMIM:Absence of frontal sinuses]
Absent frontal sinus [OMIM:Absent frontal sinus]
Absent frontal sinuses [OMIM:Absent frontal sinuses]
Frontal sinus agenesis/anomaly [Orphanet:8660]
Quality:
Cross references:
Orphanet:8660 "Frontal sinus agenesis/anomaly" [Orphanet:8660]
OMIM: "Absence of frontal sinuses" [OMIM:Absence of frontal sinuses]
OMIM: "Absent frontal sinus" [OMIM:Absent frontal sinus]
OMIM: "Absent frontal sinuses" [OMIM:Absent frontal sinuses]
Is a (Direct Parents):
Orphanet Abnormality of the nose
HPO         Aplasia/Hypoplasia of the frontal sinuses
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 skull(HPO:0000929)
                Aplasia/Hypoplasia involving bones of the skull(HPO:0009116)
                   Aplasia/Hypoplasia involving the sinuses(HPO:0009120)
                      Aplasia/Hypoplasia of the frontal sinuses(HPO:0009119)
                         Absent frontal sinuses(HPO:0002688)
                Abnormality of facial skeleton(HPO:0011821)
                   Abnormality of the paranasal sinuses(HPO:0000245)
                      Aplasia/Hypoplasia involving the sinuses(HPO:0009120)
                         Aplasia/Hypoplasia of the frontal sinuses(HPO:0009119)
                            Absent frontal sinuses(HPO:0002688)
                      Abnormality of frontal sinus(HPO:0002687)
                         Aplasia/Hypoplasia of the frontal sinuses(HPO:0009119)
                            Absent frontal sinuses(HPO:0002688)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Aplasia/hypoplasia involving the skeleton(HPO:0009115)
                Aplasia/hypoplasia affecting bones of the axial skeleton(HPO:0009122)
                   Aplasia/Hypoplasia involving bones of the skull(HPO:0009116)
                      Aplasia/Hypoplasia involving the sinuses(HPO:0009120)
                         Aplasia/Hypoplasia of the frontal sinuses(HPO:0009119)
                            Absent frontal sinuses(HPO:0002688)
             Abnormal axial skeleton morphology(HPO:0009121)
                Abnormality of the skull(HPO:0000929)
                   Aplasia/Hypoplasia involving bones of the skull(HPO:0009116)
                      Aplasia/Hypoplasia involving the sinuses(HPO:0009120)
                         Aplasia/Hypoplasia of the frontal sinuses(HPO:0009119)
                            Absent frontal sinuses(HPO:0002688)
                   Abnormality of facial skeleton(HPO:0011821)
                      Abnormality of the paranasal sinuses(HPO:0000245)
                         Aplasia/Hypoplasia involving the sinuses(HPO:0009120)
                            Aplasia/Hypoplasia of the frontal sinuses(HPO:0009119)
                               Absent frontal sinuses(HPO:0002688)
                         Abnormality of frontal sinus(HPO:0002687)
                            Aplasia/Hypoplasia of the frontal sinuses(HPO:0009119)
                               Absent frontal sinuses(HPO:0002688)
                Aplasia/hypoplasia affecting bones of the axial skeleton(HPO:0009122)
                   Aplasia/Hypoplasia involving bones of the skull(HPO:0009116)
                      Aplasia/Hypoplasia involving the sinuses(HPO:0009120)
                         Aplasia/Hypoplasia of the frontal sinuses(HPO:0009119)
                            Absent frontal sinuses(HPO:0002688)
MedDRA:
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
CILIARY DYSKINESIA, PRIMARY, 1 (OMIM:244400)
CLEIDOCRANIAL DYSPLASIA (OMIM:119600)
Camptodactyly syndrome, Guadalajara type 1 (Orphanet:1327)
Cleidocranial dysplasia (Orphanet:1452)
Dysosteosclerosis (Orphanet:1782)
HAJDU-CHENEY SYNDROME (OMIM:102500)
Marshall syndrome (Orphanet:560)
Microcornea - glaucoma - absent frontal sinuses (Orphanet:2536)
Mulibrey nanism (Orphanet:2576)
Otopalatodigital syndrome type 1 (Orphanet:90650)
Pycnodysostosis (Orphanet:763)