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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] <25>
- 1:   Abnormality of metabolism/homeostasis [HP:0001939] <32>(84|78) (91|39|15)
- 1:   Abnormality of the musculature [HP:0003011] <25>(43|52) (46|24|8)
- 1:   Abnormality of the endocrine system [HP:0000818] <14>(25|22) (29|8|4)
- 1:   Abnormality of prenatal development or birth [HP:0001197] <13>(6|11) (6|4|0)
- 1:   Abnormality of connective tissue [HP:0003549] <12>(18|26) (20|19|15)
- 1:   Abnormality of the voice [HP:0001608] <11>(6|5) (7|2|1)
- 1:   Abnormality of blood and blood-forming tissues [HP:0001871] <8>(28|34) (32|13|6)
- 1:   Abnormality of limbs [HP:0040064] <8>(53|57) (57|25|17)
- 1:   Abnormality of the breast [HP:0000769] <8>(2|4) (4|0|0)
- 1:   Abnormality of the ear [HP:0000598] <7>(17|23) (18|14|11)
- 1:   Abnormality of the skeletal system [HP:0000924] <7>(90|90) (97|51|34)
- 1:   Abnormality of the digestive system [HP:0025031] <6>(55|55) (65|32|10)
- 1:   Abnormality of the genitourinary system [HP:0000119] <5>(60|70) (68|23|6)
- 1:   Constitutional symptom [HP:0025142] <5>(4|4) (6|6|1)
- 1:   Growth abnormality [HP:0001507] <5>(24|27) (28|23|15)
- 1:   Abnormality of the cardiovascular system [HP:0001626] <4>(54|62) (60|37|22)
- 1:   Abnormality of the integument [HP:0001574] <4>(52|64) (58|43|18)
- 1:   Abnormality of the nervous system [HP:0000707] <4>(125|135) (137|72|29)
- 1:   Abnormality of the immune system [HP:0002715] <3>(48|53) (52|36|18)
- 1:   Abnormality of the respiratory system [HP:0002086] <3>(34|32) (38|25|21)
- 1:   Abnormality of head or neck [HP:0000152] <2>(94|110) (108|59|36)
- 1:   Abnormality of the eye [HP:0000478] <2>(54|60) (55|36|22)
- 1:   Neoplasm [HP:0002664] <2>(23|24) (27|10|3)
- 1:   Abnormality of the thoracic cavity [HP:0045027] <1>(1|0) (1|0|0)
- 1:   Abnormal cellular phenotype [HP:0025354](0|0) (0|0|0)