Beaking of vertebral bodies
Symptom Information:
Symptom ID: | HPO:0004568 | |||||||||||||
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) Abnormal axial skeleton morphology(HPO:0009121) Abnormality of the vertebral column(HPO:0000925) Abnormality of the vertebrae(HPO:0003468) Abnormal form of the vertebral bodies(HPO:0003312) Beaking of vertebral bodies(HPO:0004568) MedDRA: |
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Database Frequency: | 19 / 7739 | |||||||||||||
Resource: |
All diseases associated with this symptom:
Acromesomelic dysplasia, Maroteaux type | (Orphanet:40) |
Aspartylglucosaminuria | (Orphanet:93) |
Autosomal dominant Larsen syndrome | (Orphanet:503) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
DYGGVE-MELCHIOR-CLAUSEN DISEASE | (OMIM:223800) |
Dermato-cardio-skeletal syndrome, Borrone type | (Orphanet:1266) |
Dyggve-Melchior-Clausen disease | (Orphanet:239) |
GM1 gangliosidosis | (Orphanet:354) |
GM1 gangliosidosis type 1 | (Orphanet:79255) |
Geroderma osteodysplastica | (Orphanet:2078) |
Hurler syndrome | (Orphanet:93473) |
Mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis | (Orphanet:93279) |
Mucopolysaccharidosis type 2, severe form | (Orphanet:217085) |
OSTEOGENESIS IMPERFECTA, TYPE VI | (OMIM:613982) |
Pseudoachondroplasia | (Orphanet:750) |
SMITH-MCCORT DYSPLASIA 1 | (OMIM:607326) |
SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS | (OMIM:609616) |
Smith-McCort dysplasia | (Orphanet:178355) |
Stickler syndrome | (Orphanet:828) |