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• MP root. MP OBO captured 11 Feb 2021.   MP:0000001   (5184)
Definition: the observable morphological, physiological, behavioral and other characteristics of mammalian organisms that are manifested through development and lifespan [MGI:csmith];   [MGI annotations / genotypes]
• pigmentation phenotype     (29)
          • abnormal coat/hair pigmentation     (13)
          • abnormal skin pigmentation     (12)
          • abnormal extracutaneous pigmentation     (4)
• neoplasm     (16)
          • abnormal tumor susceptibility     (8)
          • abnormal tumor pathology     (13)
• nervous system phenotype     (117)
          • abnormal nervous system morphology     (66)
          • abnormal nervous system physiology     (51)
• renal/urinary system phenotype     (101)
          • abnormal renal/urinary system morphology     (49)
          • abnormal renal/urinary system physiology     (52)
• muscle phenotype     (27)
          • abnormal muscle physiology     (6)
          • abnormal muscle morphology     (21)
• liver/biliary system phenotype     (211)
          • abnormal hepatobiliary system morphology     (77)
          • abnormal hepatobiliary system physiology     (134)
• limbs/digits/tail phenotype     (95)
          • abnormal limb morphology     (76)
          • abnormal tail morphology     (19)
• adipose tissue phenotype     (125)
          • abnormal adipose tissue morphology     (125)
• homeostasis/metabolism phenotype     (1093)
          • amyloidosis     (1)
          • abnormal homeostasis     (827)
          • abnormal response to injury     (3)
          • abnormal metabolism     (127)
          • abnormal physiological response to xenobiotic     (212)
          • abnormal xenobiotic pharmacokinetics     (26)
• hearing/vestibular/ear phenotype     (28)
          • abnormal ear morphology     (12)
          • abnormal ear physiology     (24)
• growth/size/body region phenotype     (398)
          • abnormal head morphology     (22)
          • abnormal postnatal growth/weight/body size     (350)
          • abnormal prenatal growth/weight/body size     (2)
          • abnormal body composition     (71)
• endocrine/exocrine gland phenotype     (120)
          • abnormal gland morphology     (77)
          • abnormal gland physiology     (43)
• embryo phenotype     (3)
          • abnormal embryo development     (3)
• digestive/alimentary phenotype     (56)
          • abnormal digestive system morphology     (1)
          • abnormal digestive system physiology     (55)
• craniofacial phenotype     (110)
          • abnormal craniofacial morphology     (110)
• cellular phenotype     (101)
          • abnormal cell morphology     (24)
          • abnormal cell physiology     (77)
• cardiovascular system phenotype     (287)
          • abnormal cardiovascular system physiology     (220)
          • abnormal cardiovascular system morphology     (95)
• behavior/neurological phenotype     (1480)
          • abnormal behavior     (1480)
• immune system phenotype     (604)
          • abnormal immune system morphology     (318)
          • abnormal immune system physiology     (298)
• respiratory system phenotype     (78)
          • abnormal respiratory system morphology     (6)
          • abnormal respiratory system physiology     (72)
• reproductive system phenotype     (261)
          • abnormal reproductive system physiology     (153)
          • abnormal reproductive system morphology     (115)
• skeleton phenotype     (248)
          • abnormal skeleton physiology     (18)
          • abnormal skeleton morphology     (230)
• vision/eye phenotype     (133)
          • abnormal eye morphology     (102)
          • abnormal eye physiology     (40)
• taste/olfaction phenotype     (28)
          • abnormal gustatory system physiology     (28)
• hematopoietic system phenotype     (587)
          • abnormal hematopoietic system physiology     (49)
          • abnormal hematopoietic system morphology/development     (542)
• mortality/aging     (28)
          • abnormal induced morbidity/mortality     (2)
          • abnormal survival     (27)
• integument phenotype     (203)
          • abnormal touch/ nociception     (65)
          • abnormal skin morphology     (28)
          • abnormal skin physiology     (3)
          • abnormal skin adnexa morphology     (98)
          • abnormal skin adnexa physiology     (9)




VT:0000001 ( VT root. VT OBO version 11.3 captured 11 Feb 2021.) is numbered similarly to MP:0000001 but is over in the VT ontology (semantics may or may not be similar).

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