Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Human Phenotype Ontology

Grandparent Node:
Abnormality of the upper limb (HP:0002817)

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Parent Node:
Abnormality of the hand (HP:0001155)

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..Starting node
..Abnormal hand morphology (HP:0005922)

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Term ID:	5922
Name:	Abnormal hand morphology
Synonym:	Abnormal shape of hand
Definition:	Any structural anomaly of the hand.
Comments:
Reference:	HP:0005922
Genes and Diseases:	There are 772 terms for your input, too many to show detail here. Please try its child terms.
Child Nodes:
........Large hands (HP:0001176)
........Hand clenching (HP:0001188)
........Mitten deformity (HP:0004057)
........Curved fingers (HP:0004095) ................... HP:0004214 Curved phalanges of the 5th finger ................... HP:0009285 Curved phalanges of the 4th finger ................... HP:0009442 Curved phalanges of the 3rd finger ................... HP:0009549 Curved phalanges of the 2nd finger ................... HP:0009653 Curved thumb phalanx
........Notched hand bones (HP:0004284)
........Overmodelled hand bones (HP:0004285)
........Pointed hand bones (HP:0004287)
........Undermodelled hand bones (HP:0004292)
........Valgus hand deformity (HP:0006228)
........Short finger (HP:0009381) ................... HP:0005819 Short middle phalanx of finger ................... HP:0009237 Short 5th finger ................... HP:0009280 Short 4th finger ................... HP:0009461 Short 3rd finger ................... HP:0009536 Short 2nd finger ................... HP:0009778 Short thumb ................... HP:0009882 Short distal phalanx of finger ................... HP:0010241 Short proximal phalanx of finger
........Overlapping fingers (HP:0010557)
Sister Nodes:
..Abnormal carpal morphology (HP:0001191)
..Abnormal hand bone ossification (HP:0010660)
..Abnormal hand cortical bone morphology (HP:0005926)
..Abnormal hand diaphysis morphology (HP:0005925)
..Abnormal hand epiphysis morphology (HP:0005924)
..Abnormal hand metaphysis morphology (HP:0005923)
..Abnormal palm morphology (HP:0100871)
..Abnormality of dorsoventral patterning of the limbs (HP:0100270)
..Abnormality of finger (HP:0001167)
..Abnormality of hand joint mobility (HP:0006256)
..Abnormality of the metacarpal bones (HP:0001163)
..Abnormality of the musculature of the hand (HP:0001421)
..Aplasia/hypoplasia involving bones of the hand (HP:0005927)
..Autoamputation of digits (HP:0007460)
..Decreased finger mobility (HP:0006135)
..Deviation of the hand or of fingers of the hand (HP:0009484)
..Duplication of hand bones (HP:0004275)
..Exostoses of hand bones (HP:0004276)
..Fractured hand bones (HP:0004277)
..Joint contracture of the hand (HP:0009473)
..Osteolytic defects of the hand bones (HP:0009699)
..Short tubular bones of the hand (HP:0001248)
..Split hand (HP:0001171)
..Synostosis involving bones of the hand (HP:0004278)
..Ulnar claw (HP:0001178)
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.

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