SUPERFAMILY 1.75 HMM library and genome assignments server

Phenotypic Abnormality (PA): Phenotypic abnormality

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Root: HP Hierarchy (human phenotype with 3 sub-ontologies PA, MI, ON)

Shortest distance to current term (+ for parents, - for children) HP term [HP ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
0:   Phenotypic abnormality [HP:0000118] <21>
- 1:   Abnormality of metabolism/homeostasis [HP:0001939] <29>(51|42) (53|21|9)
- 1:   Abnormality of the endocrine system [HP:0000818] <12>(9|13) (12|4|3)
- 1:   Abnormality of connective tissue [HP:0003549] <11>(15|20) (16|9|4)
- 1:   Abnormality of the voice [HP:0001608] <11>(3|3) (3|1|1)
- 1:   Abnormality of prenatal development or birth [HP:0001197] <10>(3|5) (3|2|0)
- 1:   Abnormality of blood and blood-forming tissues [HP:0001871] <9>(15|17) (18|9|4)
- 1:   Abnormality of the breast [HP:0000769] <8>(0|0) (0|0|0)
- 1:   Abnormality of the musculature [HP:0003011] <8>(23|35) (25|14|6)
- 1:   Abnormality of the abdomen [HP:0001438] <6>(34|35) (38|17|3)
- 1:   Abnormality of the ear [HP:0000598] <6>(5|14) (7|5|3)
- 1:   Abnormality of the genitourinary system [HP:0000119] <5>(28|33) (33|12|4)
- 1:   Growth abnormality [HP:0001507] <5>(11|17) (13|9|8)
- 1:   Abnormality of the cardiovascular system [HP:0001626] <4>(28|34) (29|19|16)
- 1:   Abnormality of the immune system [HP:0002715] <3>(16|23) (19|10|3)
- 1:   Abnormality of the skeletal system [HP:0000924] <3>(56|60) (57|34|18)
- 1:   Abnormality of head and neck [HP:0000152] <2>(41|47) (50|25|17)
- 1:   Abnormality of the eye [HP:0000478] <2>(26|34) (33|29|20)
- 1:   Abnormality of the integument [HP:0001574] <2>(28|39) (34|21|8)
- 1:   Abnormality of the nervous system [HP:0000707] <2>(68|71) (74|39|13)
- 1:   Abnormality of the respiratory system [HP:0002086] <2>(20|25) (21|11|7)
- 1:   Neoplasm [HP:0002664] <2>(10|11) (12|4|2)