Flared metaphysis
Symptom Information:
Symptom ID: | HPO:0003015 | |||||||||||||||||
Synonyms: |
|
|||||||||||||||||
Quality: | ||||||||||||||||||
Cross references: |
|
|||||||||||||||||
Is a (Direct Parents): |
|
|||||||||||||||||
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) Abnormality of long bone morphology(HPO:0011314) Abnormality of the metaphyses(HPO:0000944) Metaphyseal widening(HPO:0003016) Flared metaphysis(HPO:0003015) Abnormal appendicular skeleton morphology(HPO:0011844) Abnormality of limb bone morphology(HPO:0002813) Abnormality of the metaphyses(HPO:0000944) Metaphyseal widening(HPO:0003016) Flared metaphysis(HPO:0003015) MedDRA: |
|||||||||||||||||
Database Frequency: | 44 / 7739 | |||||||||||||||||
Resource: |
All diseases associated with this symptom:
Achondroplasia | (Orphanet:15) |
Acromesomelic dysplasia, Maroteaux type | (Orphanet:40) |
Anauxetic dysplasia | (Orphanet:93347) |
Autosomal recessive malignant osteopetrosis | (Orphanet:667) |
CEREBROOCULOFACIOSKELETAL SYNDROME 4 | (OMIM:610758) |
CRANIOMETADIAPHYSEAL DYSPLASIA | (OMIM:269300) |
CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE | (OMIM:218400) |
Chondrodysplasia, Blomstrand type | (Orphanet:50945) |
Dysosteosclerosis | (Orphanet:1782) |
Dyssegmental dysplasia - glaucoma | (Orphanet:1804) |
EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 2 | (OMIM:615349) |
Frank-Ter Haar syndrome | (Orphanet:137834) |
Greenberg dysplasia | (Orphanet:1426) |
Hurler syndrome | (Orphanet:93473) |
Hypochondroplasia | (Orphanet:429) |
Kniest dysplasia | (Orphanet:485) |
Kyphomelic dysplasia | (Orphanet:1801) |
Lenz-Majewski hyperostotic dwarfism | (Orphanet:2658) |
Lethal Kniest-like dysplasia | (Orphanet:2347) |
Metaphyseal anadysplasia | (Orphanet:1040) |
Metaphyseal dysplasia - maxillary hypoplasia - brachydacty | (Orphanet:2504) |
Microcephalic osteodysplastic primordial dwarfism type 2 | (Orphanet:2637) |
Multiple epiphyseal dysplasia, with severe proximal femoral dysplasia | (Orphanet:166029) |
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1 | (OMIM:259700) |
Orofaciodigital syndrome type 2 | (Orphanet:2751) |
Osteocraniostenosis | (Orphanet:2763) |
Osteodysplasty, Melnick-Needles type | (Orphanet:2484) |
Otospondylomegaepiphyseal dysplasia | (Orphanet:1427) |
Perinatal lethal hypophosphatasia | (Orphanet:247623) |
Primordial short stature - microdontia - opalescent and rootless teeth | (Orphanet:46658) |
Rhizomelic chondrodysplasia punctata | (Orphanet:177) |
Rhizomelic chondrodysplasia punctata type 1 | (Orphanet:309789) |
Spondyloepimetaphyseal dysplasia - abnormal dentition | (Orphanet:168451) |
Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification | (Orphanet:93358) |
Spondyloepimetaphyseal dysplasia with joint laxity | (Orphanet:93359) |
Spondyloepimetaphyseal dysplasia with multiple dislocations | (Orphanet:93360) |
Spondyloepimetaphyseal dysplasia, Geneviève type | (Orphanet:168454) |
Spondyloepimetaphyseal dysplasia, Missouri type | (Orphanet:93356) |
Spondyloepimetaphyseal dysplasia, Shohat type | (Orphanet:93352) |
Spondylometaphyseal dysplasia, Kozlowski type | (Orphanet:93314) |
Stüve-Wiedemann syndrome | (Orphanet:3206) |
THANATOPHORIC DYSPLASIA, TYPE II | (OMIM:187601) |
Thanatophoric dysplasia type 1 | (Orphanet:1860) |
Weaver syndrome | (Orphanet:3447) |