Sclerosis of skull base

Symptom Information:

Symptom ID: HPO:0002694
Synonyms:
Marked sclerosis of skull base [HPO:0002694]
Sclerosis of the skull base [HPO:0002694]
Sclerotic of skull base [HPO:0002694]
Marked sclerosis of skull base [OMIM:Marked sclerosis of skull base]
Sclerosis of skull base [OMIM:Sclerosis of skull base]
Sclerosis of the skull base [OMIM:Sclerosis of the skull base]
Quality:
Cross references:
OMIM: "Marked sclerosis of skull base" [OMIM:Marked sclerosis of skull base]
OMIM: "Sclerosis of skull base" [OMIM:Sclerosis of skull base]
OMIM: "Sclerosis of the skull base" [OMIM:Sclerosis of the skull base]
Is a (Direct Parents):
HPO         Abnormality of the skull base
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)
                Abnormality of the skull base(HPO:0002693)
                   Sclerosis of skull base(HPO:0002694)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal axial skeleton morphology(HPO:0009121)
                Abnormality of the skull(HPO:0000929)
                   Abnormality of the skull base(HPO:0002693)
                      Sclerosis of skull base(HPO:0002694)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

Camurati-Engelmann disease (Orphanet:1328)
Craniometaphyseal dysplasia (Orphanet:1522)
Dysosteosclerosis (Orphanet:1782)
Greenberg dysplasia (Orphanet:1426)
Hurler syndrome (Orphanet:93473)
Lateral meningocele syndrome (Orphanet:2789)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Otopalatodigital syndrome (Orphanet:669)
Schinzel-Giedion syndrome (Orphanet:798)
Spondylometaphyseal dysplasia, Golden type (Orphanet:168544)