Cranial hyperostosis
Symptom Information:
Symptom ID: | HPO:0004437 | ||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) 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) 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) MedDRA: |
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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) |