Abnormality of the vertebrae

Symptom Information:

Symptom ID: HPO:0003468
Synonyms:
Abnormal vertebral bodies [HPO:0003468]
MULTIPLE VERTEBRAL ANOMALIES [HPO:0003468]
Vertebral anomalies [HPO:0003468]
Vertebra anomaly [Orphanet:16000]
Abnormal vertebral bodies [OMIM:Abnormal vertebral bodies]
Multiple vertebral anomalies [OMIM:Multiple vertebral anomalies]
Vertebral anomalies [OMIM:Vertebral anomalies]
Anomalies of spine, vertebrae and pelvis [Orphanet:16000]
Abnormal vertebral bodies (ovoid, flat, beaked) [OMIM:Abnormal vertebral bodies (ovoid, flat, beaked)]
Quality:
Cross references:
Orphanet:16000 "Anomalies of spine, vertebrae and pelvis" [Orphanet:16000]
OMIM: "Abnormal vertebral bodies" [OMIM:Abnormal vertebral bodies]
OMIM: "Multiple vertebral anomalies" [OMIM:Multiple vertebral anomalies]
OMIM: "Vertebral anomalies" [OMIM:Vertebral anomalies]
OMIM: "Abnormal vertebral bodies (ovoid, flat, beaked)" [OMIM:Abnormal vertebral bodies (ovoid, flat, beaked)]
Is a (Direct Parents):
Orphanet Abnormality of the vertebral column
HPO         Abnormality of the vertebral column
HPO         Schmorl's node
HPO         Abnormal number of vertebrae
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)
MedDRA:
Database Frequency: 77 / 7739
Resource:

All diseases associated with this symptom:

3MC SYNDROME 2 (OMIM:265050)
Aarskog-Scott syndrome (Orphanet:915)
Acrofacial dysostosis, Palagonia type (Orphanet:1787)
Acromicric dysplasia (Orphanet:969)
Acropectorovertebral dysplasia (Orphanet:957)
Adamantinoma (Orphanet:55881)
Alagille syndrome due to 20p12 microdeletion (Orphanet:261600)
Alagille syndrome due to a JAG1 point mutation (Orphanet:261619)
Alkaptonuria (Orphanet:56)
Alopecia-intellectual deficit syndrome (Orphanet:2850)
Alpha-mannosidosis (Orphanet:61)
Alveolar echinococcosis (Orphanet:284)
Ankylosing vertebral hyperostosis with tylosis (Orphanet:2206)
Autosomal recessive multiple pterygium syndrome (Orphanet:2990)
BRESEK syndrome (Orphanet:85284)
Baller-Gerold syndrome (Orphanet:1225)
Bohring-Opitz syndrome (Orphanet:97297)
Bone dysplasia, lethal Holmgren type (Orphanet:1842)
Camurati-Engelmann disease (Orphanet:1328)
Chronic recurrent multifocal osteomyelitis (Orphanet:324964)
Cobb syndrome (Orphanet:53721)
Coffin-Siris syndrome (Orphanet:1465)
Congenital cataracts - facial dysmorphism - neuropathy (Orphanet:48431)
Dysspondyloenchondromatosis (Orphanet:85198)
Embryofetopathy due to oral anticoagulant therapy (Orphanet:1914)
FANCONI ANEMIA, COMPLEMENTATION GROUP B (OMIM:300514)
Familial multiple nevi flammei (Orphanet:624)
Fetal hydantoin syndrome (Orphanet:1912)
Fibrodysplasia ossificans progressiva (Orphanet:337)
GAPO syndrome (Orphanet:2067)
Galactosialidosis (Orphanet:351)
Goldenhar syndrome (Orphanet:374)
HEMANGIOMATOSIS, CUTANEOUS, WITH ASSOCIATED FEATURES (OMIM:234800)
Haim-Munk syndrome (Orphanet:2342)
Holoprosencephaly - radial heart renal anomalies (Orphanet:3186)
Holt-Oram syndrome (Orphanet:392)
Hydatidosis (Orphanet:400)
Hypertelorism-microtia-facial clefting syndrome (Orphanet:2213)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Infantile myofibromatosis (Orphanet:2591)
Isolated Klippel-Feil syndrome (Orphanet:2345)
Joubert syndrome (Orphanet:475)
Joubert syndrome with ocular defect (Orphanet:220493)
KABUKI SYNDROME 1 (OMIM:147920)
Kabuki syndrome (Orphanet:2322)
Keratoderma hereditarium mutilans (Orphanet:494)
Lethal multiple pterygium syndrome (Orphanet:33108)
MULTIPLE SYNOSTOSES SYNDROME 1 (OMIM:186500)
Madelung deformity (Orphanet:35688)
Melhem-Fahl syndrome (Orphanet:2482)
Mesomelia-synostoses syndrome (Orphanet:2496)
Metaphyseal chondrodysplasia, Schmid type (Orphanet:174)
Monomelic amyotrophy (Orphanet:65684)
Monosomy 9p (Orphanet:261112)
Multiple synostoses syndrome (Orphanet:3237)
Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency (Orphanet:88639)
Non-rhizomelic chondrodysplasia punctata (Orphanet:176)
Osteopetrosis (Orphanet:2781)
Otopalatodigital syndrome type 1 (Orphanet:90650)
Otopalatodigital syndrome type 2 (Orphanet:90652)
Pacman dysplasia (Orphanet:1952)
Papillon-Lefèvre syndrome (Orphanet:678)
Poland syndrome (Orphanet:2911)
Primary basilar impression (Orphanet:2285)
Progeria - short stature - pigmented nevi (Orphanet:2959)
Progressive non-infectious anterior vertebral fusion (Orphanet:2062)
Pycnodysostosis (Orphanet:763)
SACRAL AGENESIS WITH VERTEBRAL ANOMALIES (OMIM:615709)
SAPHO syndrome (Orphanet:793)
Townes-Brocks syndrome (Orphanet:857)
Treacher-Collins syndrome (Orphanet:861)
Trisomy 13 (Orphanet:3378)
VACTERL ASSOCIATION WITH HYDROCEPHALUS (OMIM:276950)
VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS (OMIM:314390)
VACTERL with hydrocephalus (Orphanet:3412)
VACTERL/VATER association (Orphanet:887)
Wolf-Hirschhorn syndrome (Orphanet:280)