Cranial hyperostosis

Symptom Information:

Symptom ID: HPO:0004437
Synonyms:
Hyperostosis of cranial vault [HPO:0004437]
Cranial hyperostosis [OMIM:Cranial hyperostosis]
Hyperostosis of cranial vault [OMIM:Hyperostosis of cranial vault]
Dense/thickened skull/calvarium/cranial/facial hyperostosis [Orphanet:2520]
Cranial hyperostosis (onset in infancy) [OMIM:Cranial hyperostosis (onset in infancy)]
Quality:
Cross references:
HPO:0000250 "Dense calvaria" [Orphanet:2520]
HPO:0002684 "Thickened calvaria" [Orphanet:2520]
HPO:0004490 "Calvarial hyperostosis" [Orphanet:2520]
Orphanet:2520 "Dense/thickened skull/calvarium/cranial/facial hyperostosis" [Orphanet:2520]
OMIM: "Cranial hyperostosis" [OMIM:Cranial hyperostosis]
OMIM: "Hyperostosis of cranial vault" [OMIM:Hyperostosis of cranial vault]
OMIM: "Cranial hyperostosis (onset in infancy)" [OMIM:Cranial hyperostosis (onset in infancy)]
Is a (Direct Parents):
Orphanet Dense calvaria
HPO         Hyperostosis
Orphanet Abnormality of the skull
HPO         Abnormality of the calvaria
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 calvaria(HPO:0002683)
                   Cranial hyperostosis(HPO:0004437)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Hyperostosis(HPO:0100774)
                Cranial hyperostosis(HPO:0004437)
             Abnormal axial skeleton morphology(HPO:0009121)
                Abnormality of the skull(HPO:0000929)
                   Abnormality of the calvaria(HPO:0002683)
                      Cranial hyperostosis(HPO:0004437)
MedDRA:
Database Frequency: 55 / 7739
Resource:

All diseases associated with this symptom:

AREDYLD syndrome (Orphanet:1133)
Acromegaloid facial appearance syndrome (Orphanet:965)
Acroosteolysis, dominant type (Orphanet:955)
Albright hereditary osteodystrophy (Orphanet:665)
Alpha-mannosidosis (Orphanet:61)
Aspartylglucosaminuria (Orphanet:93)
Autosomal dominant osteosclerosis, Worth type (Orphanet:2790)
Blepharophimosis - radioulnar synostosis (Orphanet:1256)
CLOVE syndrome (Orphanet:140944)
CRANIODIAPHYSEAL DYSPLASIA (OMIM:218300)
CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE (OMIM:218400)
Caffey disease (Orphanet:1310)
Chondrodysplasia - disorder of sex development (Orphanet:1422)
Coffin-Lowry syndrome (Orphanet:192)
Craniodiaphyseal dysplasia (Orphanet:1513)
Craniometaphyseal dysplasia (Orphanet:1522)
Dysosteosclerosis (Orphanet:1782)
Ectodermal dysplasia with natal teeth, Turnpenny type (Orphanet:69083)
Encephalocraniocutaneous lipomatosis (Orphanet:2396)
Eye defects - arachnodactyly - cardiopathy (Orphanet:2725)
Fountain syndrome (Orphanet:3219)
Frontometaphyseal dysplasia (Orphanet:1826)
Ghosal hematodiaphyseal dysplasia (Orphanet:1802)
HYPEROSTOSIS CORTICALIS GENERALISATA (OMIM:239100)
Hidrotic ectodermal dysplasia (Orphanet:189)
Hyperostosis corticalis generalisata (Orphanet:3416)
Intellectual deficit - myopathy - short stature - endocrine defect (Orphanet:3068)
Juvenile Paget disease (Orphanet:2801)
Lateral meningocele syndrome (Orphanet:2789)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
Marshall syndrome (Orphanet:560)
Metaphyseal chondrodysplasia, Jansen type (Orphanet:33067)
Metaphyseal dysplasia - maxillary hypoplasia - brachydacty (Orphanet:2504)
Mucolipidosis type 3 (Orphanet:577)
Mucopolysaccharidosis type 3 (Orphanet:581)
Myhre syndrome (Orphanet:2588)
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2 (OMIM:259710)
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3 (OMIM:259730)
Oculodentodigital dysplasia (Orphanet:2710)
Osteodysplasty, Melnick-Needles type (Orphanet:2484)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Osteopetrosis with renal tubular acidosis (Orphanet:2785)
Osteosclerosis - developmental delay - craniosynostosis (Orphanet:178377)
Otopalatodigital syndrome (Orphanet:669)
Otopalatodigital syndrome type 1 (Orphanet:90650)
Otopalatodigital syndrome type 2 (Orphanet:90652)
Proteus syndrome (Orphanet:744)
Pseudoleprechaunism syndrome, Patterson type (Orphanet:2976)
Pyle disease (Orphanet:3005)
SCLEROSTEOSIS 1 (OMIM:269500)
SPONASTRIME dysplasia (Orphanet:93357)
Sclerosteosis (Orphanet:3152)
Tricho-dento-osseous syndrome (Orphanet:3352)
X-linked hypophosphatemia (Orphanet:89936)
Xeroderma pigmentosum (Orphanet:910)