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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] <23>
- 1:   Abnormality of metabolism/homeostasis [HP:0001939] <31>(84|77) (92|40|14)
- 1:   Abnormality of the musculature [HP:0003011] <23>(42|50) (45|25|8)
- 1:   Abnormality of the endocrine system [HP:0000818] <14>(24|23) (29|8|4)
- 1:   Abnormality of connective tissue [HP:0003549] <12>(18|24) (20|20|14)
- 1:   Abnormality of prenatal development or birth [HP:0001197] <11>(6|10) (6|4|0)
- 1:   Abnormality of the voice [HP:0001608] <11>(6|5) (7|2|1)
- 1:   Abnormality of the skeletal system [HP:0000924] <10>(90|87) (96|52|32)
- 1:   Abnormality of blood and blood-forming tissues [HP:0001871] <8>(28|33) (30|13|6)
- 1:   Abnormality of limbs [HP:0040064] <8>(53|54) (57|25|16)
- 1:   Abnormality of the breast [HP:0000769] <8>(1|5) (4|0|0)
- 1:   Abnormality of the ear [HP:0000598] <7>(15|23) (17|16|11)
- 1:   Abnormality of the digestive system [HP:0025031] <6>(55|55) (65|35|10)
- 1:   Abnormality of the genitourinary system [HP:0000119] <5>(60|66) (67|24|5)
- 1:   Growth abnormality [HP:0001507] <5>(23|27) (26|21|14)
- 1:   Abnormality of the cardiovascular system [HP:0001626] <4>(51|63) (58|37|22)
- 1:   Abnormality of the nervous system [HP:0000707] <4>(127|136) (140|77|31)
- 1:   Abnormality of the immune system [HP:0002715] <3>(48|52) (51|36|17)
- 1:   Abnormality of the integument [HP:0001574] <3>(51|62) (58|42|14)
- 1:   Abnormality of the respiratory system [HP:0002086] <3>(33|34) (39|25|20)
- 1:   Abnormality of head or neck [HP:0000152] <2>(95|107) (109|60|33)
- 1:   Abnormality of the eye [HP:0000478] <2>(55|59) (55|37|20)
- 1:   Neoplasm [HP:0002664] <2>(23|27) (25|10|3)
- 1:   Abnormality of the thoracic cavity [HP:0045027] <1>(1|0) (1|0|0)