Metaphyseal irregularity
Symptom Information:
Symptom ID: | HPO:0003025 | ||||||||||||
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 appendicular skeleton morphology(HPO:0011844) Abnormality of limb bone morphology(HPO:0002813) Abnormality of the metaphyses(HPO:0000944) Metaphyseal irregularity(HPO:0003025) Abnormality of long bone morphology(HPO:0011314) Abnormality of the metaphyses(HPO:0000944) Metaphyseal irregularity(HPO:0003025) MedDRA: |
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Database Frequency: | 42 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
Dent disease type 1 | (Orphanet:93622) |
EPIPHYSEAL DYSPLASIA, BAUMANN TYPE | (OMIM:610797) |
Free sialic acid storage disease, infantile form | (Orphanet:309324) |
HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE | (OMIM:300554) |
Hereditary hypophosphatemic rickets with hypercalciuria | (Orphanet:157215) |
Hypocalcemic vitamin D-dependent rickets | (Orphanet:289157) |
Hypocalcemic vitamin D-resistant rickets | (Orphanet:93160) |
Jeune syndrome | (Orphanet:474) |
Lethal Kniest-like dysplasia | (Orphanet:2347) |
METAPHYSEAL ANADYSPLASIA 2 | (OMIM:613073) |
METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS | (OMIM:250460) |
Metaphyseal chondrodysplasia, Kaitila type | (Orphanet:166038) |
Metaphyseal dysostosis - intellectual deficit - conductive deafness | (Orphanet:2502) |
Mucopolysaccharidosis type 6 | (Orphanet:583) |
Multiple epiphyseal dysplasia type 5 | (Orphanet:93311) |
Neonatal severe primary hyperparathyroidism | (Orphanet:417) |
Orofaciodigital syndrome type 2 | (Orphanet:2751) |
SMITH-MCCORT DYSPLASIA 1 | (OMIM:607326) |
SPONASTRIME dysplasia | (Orphanet:93357) |
SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION | (OMIM:607944) |
Schneckenbecken dysplasia | (Orphanet:3144) |
Short-rib thoracic dysplasia 1 with or without polydactyly | (OMIM:208500) |
Smith-McCort dysplasia | (Orphanet:178355) |
Spondylo-megaepiphyseal-metaphyseal dysplasia | (Orphanet:228387) |
Spondyloepimetaphyseal dysplasia - abnormal dentition | (Orphanet:168451) |
Spondyloepimetaphyseal dysplasia congenita, Strudwick type | (Orphanet:93346) |
Spondyloepimetaphyseal dysplasia with multiple dislocations | (Orphanet:93360) |
Spondyloepimetaphyseal dysplasia, Geneviève type | (Orphanet:168454) |
Spondyloepimetaphyseal dysplasia, Shohat type | (Orphanet:93352) |
Spondylometaphyseal dysplasia - cone-rod dystrophy | (Orphanet:85167) |
Spondylometaphyseal dysplasia, 'corner fracture' type | (Orphanet:93315) |
Spondylometaphyseal dysplasia, A4 type | (Orphanet:168555) |
Spondylometaphyseal dysplasia, Kozlowski type | (Orphanet:93314) |
Spondylometaphyseal dysplasia, Sedaghatian type | (Orphanet:93317) |
THANATOPHORIC DYSPLASIA, TYPE II | (OMIM:187601) |
Thanatophoric dysplasia type 1 | (Orphanet:1860) |
VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A | (OMIM:264700) |
VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B | (OMIM:600081) |
VITAMIN D-DEPENDENT RICKETS, TYPE 2A | (OMIM:277440) |
VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR | (OMIM:600785) |
X-linked hypophosphatemia | (Orphanet:89936) |
X-linked spondyloepimetaphyseal dysplasia | (Orphanet:93349) |