Thickened calvaria
Symptom Information:
Symptom ID: | HPO:0002684 | |||||||||||||||||||||||||
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 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) 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) MedDRA: |
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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) |