Human Phenotype Ontology 
Grandparent Node:
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All (HP:0000001)help
Parent Node:
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Phenotypic abnormality (HP:0000118)help
..Starting node
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Abnormality of limbs (HP:0040064)help
Term ID: 40064
Name: Abnormality of limbs
Synonym: Abnormal limbs; Abnormality of limbs; Dysmelia; Limb anomaly
Definition:
Comments:
Reference: HP:0040064
Genes and Diseases:There are 2854 terms for your input, too many to show detail here. Please try its child terms.
 
       Child Nodes:
........expandAutoamputation (HP:0001218) help
................... HP:0001868 Autoamputation of foot
................... HP:0007460 Autoamputation of digits
........expandHemihypertrophy (HP:0001528) help
................... HP:0100553 Hemihypertrophy of lower limb
................... HP:0100554 Hemihypertrophy of upper limb
........expandAbnormality of the lower limb (HP:0002814) help
................... HP:0001437 Abnormality of the musculature of the lower limbs
................... HP:0001760 Abnormality of the foot
................... HP:0002522 Areflexia of lower limbs
................... HP:0002600 Hyporeflexia of lower limbs
................... HP:0002981 Abnormality of the calf
................... HP:0003783 Externally rotated/abducted legs
................... HP:0006463 Rickets of the lower limbs
................... HP:0006490 Abnormality of lower-limb metaphyses
................... HP:0006500 Abnormality of lower limb epiphysis morphology
................... HP:0009053 Distal lower limb muscle weakness
................... HP:0010495 Amniotic constriction rings of legs
................... HP:0010496 Hypertrophy of the lower limb
................... HP:0010497 Sirenomelia
................... HP:0010741 Edema of the lower limbs
................... HP:0040069 Abnormality of lower limb bone
................... HP:0100491 Abnormality of lower limb joint
................... HP:0100559 Lower limb asymmetry
........expandAbnormality of the upper limb (HP:0002817) help
................... HP:0001155 Abnormality of the hand
................... HP:0001446 Abnormality of the musculature of the upper limbs
................... HP:0001454 Abnormality of the upper arm
................... HP:0002973 Abnormality of the forearm
................... HP:0003839 Abnormality of upper limb epiphysis morphology
................... HP:0006488 Bowing of the arm
................... HP:0006496 Aplasia/hypoplasia involving bones of the upper limbs
................... HP:0008959 Distal upper limb muscle weakness
................... HP:0009142 Duplication of bones involving the upper extremities
................... HP:0009808 Anomaly of the upper limb diaphyses
................... HP:0009809 Abnormality of upper limb metaphysis
................... HP:0009810 Abnormality of upper limb joint
................... HP:0010483 Amniotic constriction rings of arms
................... HP:0010484 Hypertrophy of the upper limb
................... HP:0010742 Edema of the upper limbs
................... HP:0012046 Areflexia of upper limbs
................... HP:0012391 Hyporeflexia of upper limbs
................... HP:0012769 Abnormal arm span
................... HP:0040070 Abnormality of upper limb bone
................... HP:0100560 Upper limb asymmetry
........expandLimb fasciculations (HP:0007289) help
........expandAbnormality of the musculature of the limbs (HP:0009127) help
................... HP:0001437 Abnormality of the musculature of the lower limbs
................... HP:0001446 Abnormality of the musculature of the upper limbs
................... HP:0002509 Limb hypertonia
................... HP:0003325 Limb-girdle muscle weakness
................... HP:0003690 Limb muscle weakness
................... HP:0003797 Limb-girdle muscle atrophy
................... HP:0007066 Proximal limb muscle stiffness
................... HP:0007156 Asymmetric limb muscle stiffness
................... HP:0009028 Generalized weakness of limb muscles
................... HP:0009128 Aplasia/Hypoplasia involving the musculature of the extremities
........expandAplasia/hypoplasia of the extremities (HP:0009815) help
................... HP:0009826 Limb undergrowth
................... HP:0009827 Amelia
................... HP:0009828 Peromelia
................... HP:0009829 Phocomelia
................... HP:0010884 Acromelia
................... HP:0045060 Aplasia/hypoplasia involving bones of the extremities
........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

 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 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 skeletal system (HP:0000924) 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.