Human Phenotype Ontology 
Grandparent Node:
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Phenotypic abnormality (HP:0000118)help
Parent Node:
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Abnormality of the skeletal system (HP:0000924)help
..Starting node
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Abnormality of skeletal morphology (HP:0011842)help
Term ID: 11842
Name: Abnormality of skeletal morphology
Synonym: Abnormally shaped skeletal
Definition: An abnormality of the form, structure, or size of the skeletal system.
Comments:
Reference: HP:0011842
Genes and Diseases:There are 3606 terms for your input, too many to show detail here. Please try its child terms.
 
       Child Nodes:
........expandDysostosis multiplex (HP:0000943) help
........expandAbnormal joint morphology (HP:0001367) help
................... HP:0000934 Chondrocalcinosis
................... HP:0001059 Pterygium
................... HP:0001369 Arthritis
................... HP:0001373 Joint dislocation
................... HP:0001386 Joint swelling
................... HP:0003037 Enlarged joints
................... HP:0003040 Arthropathy
................... HP:0005187 Progressive joint destruction
................... HP:0005261 Joint hemorrhage
................... HP:0005262 Abnormality of the synovia
................... HP:0009810 Abnormality of upper limb joint
................... HP:0011729 Abnormality of joint mobility
................... HP:0040188 Osteochondrosis
................... HP:0100491 Abnormality of lower limb joint
................... HP:0100781 Abnormality of the sacroiliac joint
........expandSkeletal dysplasia (HP:0002652) help
................... HP:0002651 Spondyloepimetaphyseal dysplasia
................... HP:0002654 Multiple epiphyseal dysplasia
................... HP:0002655 Spondyloepiphyseal dysplasia
................... HP:0002656 Epiphyseal dysplasia
................... HP:0002657 Spondylometaphyseal dysplasia
................... HP:0005716 Lethal skeletal dysplasia
................... HP:0005775 Multiple skeletal anomalies
................... HP:0100252 Diaphyseal dysplasia
................... HP:0100255 Metaphyseal dysplasia
........expandAbnormal cartilage morphology (HP:0002763) help
................... HP:0005701 Multiple enchondromatosis
................... HP:0008178 Abnormal cartilage matrix
................... HP:0008271 Abnormal cartilage collagen
................... HP:0100593 Calcification of cartilage
................... HP:0100662 Chondritis
................... HP:0100773 Cartilage destruction
........expandAbnormal bone structure (HP:0003330) help
................... HP:0002797 Osteolysis
................... HP:0003103 Abnormal cortical bone morphology
................... HP:0003961 Fractured forearm bones
................... HP:0003976 Constricted radius
................... HP:0006433 Dysplastic radii
................... HP:0006446 Dysplastic patella
................... HP:0010734 Fibrous dysplasia of the bones
................... HP:0011849 Abnormal bone ossification
................... HP:0011862 Abnormal bone collagen fibril morphology
................... HP:0012062 Bone cyst
................... HP:0030313 Abnormal periosteum morphology
................... HP:0100671 Abnormal trabecular bone morphology
........expandAplasia/hypoplasia involving the skeleton (HP:0009115) help
................... HP:0009122 Aplasia/hypoplasia affecting bones of the axial skeleton
................... HP:0009815 Aplasia/hypoplasia of the extremities
........expandAbnormal axial skeleton morphology (HP:0009121) help
................... HP:0000765 Abnormality of the thorax
................... HP:0000925 Abnormality of the vertebral column
................... HP:0000929 Abnormality of the skull
................... HP:0003521 Disproportionate short-trunk short stature
................... HP:0009122 Aplasia/hypoplasia affecting bones of the axial skeleton
................... HP:0009144 Supernumerary bones of the axial skeleton
........expandNeoplasm of the skeletal system (HP:0010622) help
................... HP:0002669 Osteosarcoma
................... HP:0006765 Chondrosarcoma
................... HP:0010762 Chordoma
................... HP:0011846 Osteoblastoma
................... HP:0011847 Giant cell tumor of bone
................... HP:0030038 Enchondroma
................... HP:0030431 Osteochondroma
................... HP:0030432 Chondroblastoma
................... HP:0100246 Osteoma
................... HP:0100777 Exostoses
........expandAbnormal appendicular skeleton morphology (HP:0011844) help
................... HP:0002644 Abnormality of pelvic girdle bone morphology
................... HP:0002813 Abnormality of limb bone morphology
................... HP:0003043 Abnormality of the shoulder
................... HP:0011314 Abnormality of long bone morphology
........expandAbnormality of synovial bursa morphology (HP:0025231) help
................... HP:0025232 Bursitis
........expandAbnormality of growth plate morphology (HP:0025368) help
................... HP:0025369 Thick growth plates
........expandHyperplastic callus formation (HP:0030268) help
........expandAbnormal tendon morphology (HP:0100261) help
................... HP:0001371 Flexion contracture
................... HP:0005109 Abnormality of the Achilles tendon
................... HP:0010874 Tendon xanthomatosis
................... HP:0012276 Digital flexor tenosynovitis
................... HP:0025230 Tendonitis
................... HP:0100550 Tendon rupture
........expandHyperostosis (HP:0100774) help
................... HP:0004437 Cranial hyperostosis
................... HP:0008442 Vertebral hyperostosis
........expandAbnormality of cartilage morphology (HP:0410007) help
................... HP:3000022 Abnormality of cartilage of external ear
................... HP:3000034 Abnormality of cartilage of nasal septum
................... HP:3000038 Abnormal cricoid cartilage morphology
........expandAbnormality of hyoid bone (HP:3000052) help
........expandAbnormality of mandibular symphysis (HP:3000079) help

 Sister Nodes: 
..expandAbnormal odontoid tissue morphology (HP:3000050) help
..expandAbnormality of limb bone (HP:0040068) help
..expandAbnormality of musculoskeletal physiology (HP:0011843) help
..expandAbnormality of the nasal skeleton (HP:0010937) help
..expandAbnormality of the periosteum (HP:0040166) help
..expandEctopic calcification (HP:0010766) help


Genes (0) :

Diseases (0) :
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.