Human Phenotype Ontology 
Grandparent Node:
expand
All (HP:0000001)help
Parent Node:
expand
Phenotypic abnormality (HP:0000118)help
..Starting node
..expand
Abnormality of the skeletal system (HP:0000924)help
Term ID: 924
Name: Abnormality of the skeletal system
Synonym: Abnormality of the skeletal system; Skeletal abnormalities; Skeletal anomalies
Definition: An abnormality of the skeletal system.
Comments:
Reference: HP:0000924
Genes and Diseases:There are 3804 terms for your input, too many to show detail here. Please try its child terms.
 
       Child Nodes:
........expandEctopic calcification (HP:0010766) help
................... HP:0000934 Chondrocalcinosis
................... HP:0002514 Cerebral calcification
................... HP:0002787 Tracheal calcification
................... HP:0002832 Calcific stippling
................... HP:0005213 Pancreatic calcification
................... HP:0005645 Intervertebral disk calcification
................... HP:0006514 Intraalveolar nodular calcifications
................... HP:0006559 Hepatic calcification
................... HP:0006637 Sternal punctate calcifications
................... HP:0007352 Cerebellar calcifications
................... HP:0007618 Subcutaneous calcification
................... HP:0007862 Retinal calcification
................... HP:0008131 Tarsal stippling
................... HP:0008420 Punctate vertebral calcifications
................... HP:0008703 Gonadal calcification
................... HP:0008754 Laryngeal calcification
................... HP:0009164 Abnormal calcification of the carpal bones
................... HP:0010512 Adrenal calcification
................... HP:0010655 Epiphyseal stippling
................... HP:0011915 Cardiovascular calcification
................... HP:0025141 Gingival calcification
................... HP:0025477 Periarticular calcification
................... HP:0025520 Calcinosis cutis
................... HP:0040059 Calcification of ribs
................... HP:0100249 Calcification of muscles
................... HP:0100593 Calcification of cartilage
........expandAbnormality of the nasal skeleton (HP:0010937) help
................... HP:0010939 Abnormality of the nasal bone
................... HP:3000034 Abnormality of cartilage of nasal septum
........expandAbnormality of skeletal morphology (HP:0011842) help
................... HP:0000943 Dysostosis multiplex
................... HP:0001367 Abnormal joint morphology
................... HP:0002652 Skeletal dysplasia
................... HP:0002763 Abnormal cartilage morphology
................... HP:0003330 Abnormal bone structure
................... HP:0009115 Aplasia/hypoplasia involving the skeleton
................... HP:0009121 Abnormal axial skeleton morphology
................... HP:0010622 Neoplasm of the skeletal system
................... HP:0011844 Abnormal appendicular skeleton morphology
................... HP:0025231 Abnormality of synovial bursa morphology
................... HP:0025368 Abnormality of growth plate morphology
................... HP:0030268 Hyperplastic callus formation
................... HP:0100261 Abnormal tendon morphology
................... HP:0100774 Hyperostosis
................... HP:0410007 Abnormality of cartilage morphology
................... HP:3000052 Abnormality of hyoid bone
................... HP:3000079 Abnormality of mandibular symphysis
........expandAbnormality of skeletal physiology (HP:0011843) help
................... HP:0000927 Abnormality of skeletal maturation
................... HP:0002653 Bone pain
................... HP:0002659 Increased susceptibility to fractures
................... HP:0002754 Osteomyelitis
................... HP:0009763 Limb pain
................... HP:0010885 Aseptic necrosis
........expandAbnormality of limb bone (HP:0040068) help
................... HP:0002813 Abnormality of limb bone morphology
................... HP:0040069 Abnormality of lower limb bone
................... HP:0040070 Abnormality of upper limb bone
........expandAbnormality of the periosteum (HP:0040166) help
................... HP:0030313 Abnormal periosteum morphology
........expandAbnormality of odontoid tissue (HP:3000050) help
................... HP:0000682 Abnormality of dental enamel
................... HP:0000703 Dentinogenesis imperfecta
................... HP:0100717 Abnormality of the cementum

 Sister Nodes: 
..expandAbnormal cellular phenotype (HP:0025354) help
..expandAbnormality of blood and blood-forming tissues (HP:0001871) help
..expandAbnormality of connective tissue (HP:0003549) help
..expandAbnormality of head or neck (HP:0000152) help
..expandAbnormality of limbs (HP:0040064) help
..expandAbnormality of metabolism/homeostasis (HP:0001939) help
..expandAbnormality of prenatal development or birth (HP:0001197) help
..expandAbnormality of the breast (HP:0000769) help
..expandAbnormality of the cardiovascular system (HP:0001626) help
..expandAbnormality of the digestive system (HP:0025031) help
..expandAbnormality of the ear (HP:0000598) help
..expandAbnormality of the endocrine system (HP:0000818) help
..expandAbnormality of the eye (HP:0000478) help
..expandAbnormality of the genitourinary system (HP:0000119) help
..expandAbnormality of the immune system (HP:0002715) help
..expandAbnormality of the integument (HP:0001574) help
..expandAbnormality of the musculature (HP:0003011) help
..expandAbnormality of the nervous system (HP:0000707) help
..expandAbnormality of the respiratory system (HP:0002086) help
..expandAbnormality of the thoracic cavity (HP:0045027) help
..expandAbnormality of the voice (HP:0001608) help
..expandConstitutional symptom (HP:0025142) help
..expandGrowth abnormality (HP:0001507) help
..expandNeoplasm (HP:0002664) help
..expandobsolete Abnormal test result (HP:0500014) help


Genes (0) :

Diseases (0) :
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.