Thickened calvaria

Symptom Information:

Symptom ID: HPO:0002684
Synonyms:
Calvarial thickening [HPO:0002684]
Calvarium thickened [HPO:0002684]
Increased calvarial thickness [HPO:0002684]
Thick calvaria [HPO:0002684]
Thick calvarium [HPO:0002684]
Thickened calcaria [HPO:0002684]
Thickened calvarium [HPO:0002684]
Thickened cranial vault [HPO:0002684]
Thickened cranium [HPO:0002684]
Thickening of the calvaria [HPO:0002684]
Cranial hyperostosis [Orphanet:2520]
Calvarial thickening [OMIM:Calvarial thickening]
Calvarium thickened [OMIM:Calvarium thickened]
Increased calvarial thickness [OMIM:Increased calvarial thickness]
Thick calvaria [OMIM:Thick calvaria]
Thick calvarium [OMIM:Thick calvarium]
Thickened calvaria [OMIM:Thickened calvaria]
Thickened calvarium [OMIM:Thickened calvarium]
Thickened cranial vault [OMIM:Thickened cranial vault]
Thickened cranium [OMIM:Thickened cranium]
Thickening of the calvaria [OMIM:Thickening of the calvaria]
Dense/thickened skull/calvarium/cranial/facial hyperostosis [Orphanet:2520]
Calvarial thickening (parietal and occipital area) [OMIM:Calvarial thickening (parietal and occipital area)]
Calvarial thickening (parietal and occipital regions) [OMIM:Calvarial thickening (parietal and occipital regions)]
Cranial hyperostosis (onset in infancy) [OMIM:Cranial hyperostosis (onset in infancy)]
Quality:
Cross references:
HPO:0004437 "Cranial hyperostosis" [Orphanet:2520]
HPO:0000250 "Dense calvaria" [Orphanet:2520]
HPO:0004490 "Calvarial hyperostosis" [Orphanet:2520]
Orphanet:2520 "Dense/thickened skull/calvarium/cranial/facial hyperostosis" [Orphanet:2520]
OMIM: "Calvarial thickening" [OMIM:Calvarial thickening]
OMIM: "Calvarium thickened" [OMIM:Calvarium thickened]
OMIM: "Increased calvarial thickness" [OMIM:Increased calvarial thickness]
OMIM: "Thick calvaria" [OMIM:Thick calvaria]
OMIM: "Thick calvarium" [OMIM:Thick calvarium]
OMIM: "Thickened calvaria" [OMIM:Thickened calvaria]
OMIM: "Thickened calvarium" [OMIM:Thickened calvarium]
OMIM: "Thickened cranial vault" [OMIM:Thickened cranial vault]
OMIM: "Thickened cranium" [OMIM:Thickened cranium]
OMIM: "Thickening of the calvaria" [OMIM:Thickening of the calvaria]
OMIM: "Calvarial thickening (parietal and occipital area)" [OMIM:Calvarial thickening (parietal and occipital area)]
OMIM: "Calvarial thickening (parietal and occipital regions)" [OMIM:Calvarial thickening (parietal and occipital regions)]
OMIM: "Cranial hyperostosis (onset in infancy)" [OMIM:Cranial hyperostosis (onset in infancy)]
Is a (Direct Parents):
HPO         Abnormality of the calvaria
Orphanet Abnormality of the skull
Orphanet Dense calvaria
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       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 calvaria(HPO:0002683)
                      Thickened calvaria(HPO:0002684)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the skull(HPO:0000929)
                Abnormality of the calvaria(HPO:0002683)
                   Thickened calvaria(HPO:0002684)
MedDRA:
Database Frequency: 32 / 7739
Resource:

All diseases associated with this symptom:

AREDYLD syndrome (Orphanet:1133)
Albright hereditary osteodystrophy (Orphanet:665)
Alpha-mannosidosis (Orphanet:61)
Aspartylglucosaminuria (Orphanet:93)
Autosomal dominant osteopetrosis type 1 (Orphanet:2783)
Borjeson-Forssman-Lehmann syndrome (Orphanet:127)
CLEIDOCRANIAL DYSPLASIA (OMIM:119600)
COCKAYNE SYNDROME A (OMIM:216400)
COCKAYNE SYNDROME B (OMIM:133540)
Cleidocranial dysplasia (Orphanet:1452)
Cockayne syndrome (Orphanet:191)
Coffin-Lowry syndrome (Orphanet:192)
Cranio-osteoarthropathy (Orphanet:1525)
DYGGVE-MELCHIOR-CLAUSEN DISEASE (OMIM:223800)
DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED (OMIM:304950)
Dyggve-Melchior-Clausen disease (Orphanet:239)
Fountain syndrome (Orphanet:3219)
Hereditary neutrophilia (Orphanet:279943)
Hurler syndrome (Orphanet:93473)
Juvenile Paget disease (Orphanet:2801)
Marshall syndrome (Orphanet:560)
Metaphyseal acroscyphodysplasia (Orphanet:1240)
Mucolipidosis type 2 (Orphanet:576)
Mucopolysaccharidosis type 2 (Orphanet:580)
Myhre syndrome (Orphanet:2588)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Pseudoleprechaunism syndrome, Patterson type (Orphanet:2976)
Pyle disease (Orphanet:3005)
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2 (OMIM:616331)
SCLEROSTEOSIS 1 (OMIM:269500)
Salla disease (Orphanet:309334)
VAN BUCHEM DISEASE, TYPE 2 (OMIM:607636)