All individuals in MeSH

Label Id Description
Herbicide Resistance D053209 [Diminished or failed response of PLANTS to HERBICIDES. ]
Herbicides D006540 [Pesticides used to destroy unwanted vegetation, especially various types of weeds, grasses (POACEAE), and woody plants. Some plants develop HERBICIDE RESISTANCE. ]
Herbivory D060434 [The act of feeding on plants by animals. ]
Hereditary Angioedema Type III D056828 [A form of hereditary angioedema that occurs in women and is precipitated or worsened by high ESTROGEN levels. It is associated with mutations in the gene for FACTOR XII that result in its increased activity. ]
Hereditary Angioedema Types I and II D056829 [Forms of hereditary angioedema that occur due to mutations in the gene for COMPLEMENT C1 INHIBITOR PROTEIN. Type I hereditary angioedema is associated with reduced serum levels of complement C1 inhibitor protein. Type II hereditary angioedema is associated with the production of a non-functional complement C1 inhibitor protein. ]
Hereditary Autoinflammatory Diseases D056660 [Hereditary inflammation conditions, characterized by recurrent episodes of systemic inflammation. Common symptoms include recurrent fever, rash, arthritis, fatigue, and secondary AMYLOIDOSIS. Hereditary autoinflammatory diseases are associated with mutations in genes involved in regulation of normal inflammatory process and are not caused by AUTOANTIBODIES, or antigen specific T-LYMPHOCYTES. ]
Hereditary Breast and Ovarian Cancer Syndrome D061325 [Autosomal dominant HEREDITARY CANCER SYNDROME in which a mutation most often in either BRCA1 or BRCA2 is associated with a significantly increased risk for breast and ovarian cancers. ]
Hereditary Central Nervous System Demyelinating Diseases D020279 [Inherited conditions characterized by a loss of MYELIN in the central nervous system. ]
Hereditary Complement Deficiency Diseases D000081208 [Genetic disorders due to mutations in genes involved in COMPLEMENT SYSTEM PROTEINS. They are often classified into distinct pathway of complement activation where causative mutations are found (e.g., classical pathway, lectin pathway, alternative pathway, and terminal complement pathway). ]
Hereditary Sensory and Autonomic Neuropathies D009477 [A group of inherited disorders characterized by degeneration of dorsal root and autonomic ganglion cells, and clinically by loss of sensation and autonomic dysfunction. There are five subtypes. Type I features autosomal dominant inheritance and distal sensory involvement. Type II is characterized by autosomal inheritance and distal and proximal sensory loss. Type III is DYSAUTONOMIA, FAMILIAL. Type IV features insensitivity to pain, heat intolerance, and mental deficiency. Type V is characterized by a selective loss of pain with intact light touch and vibratory sensation. (From Joynt, Clinical Neurology, 1995, Ch51, pp142-4) ]
Hereditary Sensory and Motor Neuropathy D015417 [A group of slowly progressive inherited disorders affecting motor and sensory peripheral nerves. Subtypes include HMSNs I-VII. HMSN I and II both refer to CHARCOT-MARIE-TOOTH DISEASE. HMSN III refers to hypertrophic neuropathy of infancy. HMSN IV refers to REFSUM DISEASE. HMSN V refers to a condition marked by a hereditary motor and sensory neuropathy associated with spastic paraplegia (see SPASTIC PARAPLEGIA, HEREDITARY). HMSN VI refers to HMSN associated with an inherited optic atrophy (OPTIC ATROPHIES, HEREDITARY), and HMSN VII refers to HMSN associated with retinitis pigmentosa. (From Adams et al., Principles of Neurology, 6th ed, p1343) ]
Heredity D040941 [The transmission of traits encoded in GENES from parent to offspring. ]
Heredodegenerative Disorders, Nervous System D020271 [Inherited disorders characterized by progressive atrophy and dysfunction of anatomically or physiologically related neurologic systems. ]
Hericium D000084824 [A genus of fungi in the family Hericiaceae, order Russulales, and phylum BASIDIOMYCOTA. Hericium fungi are basidiomycetes with distinctive white fruiting body that resembles icicles such as in lion's mane mushroom, Hericium erinaceus. ]
Hermanski-Pudlak Syndrome D022861 [Syndrome characterized by the triad of oculocutaneous albinism (ALBINISM, OCULOCUTANEOUS); PLATELET STORAGE POOL DEFICIENCY; and lysosomal accumulation of ceroid lipofuscin. ]
Hermaphroditic Organisms D057850 [Animals and plants in which both sperm and eggs are produced by the same individual but at different times. , Organisms which begin as female and later switch to male. , Organisms with both protandrous and protogynous individuals. , Organisms which begin as male and later switch to female. , Animals and plants which have, as their normal mode of reproduction, both male and female sex organs in the same individual. ]
Hermeneutics D066297 [The art, theory, and philosophy of interpreting the meaning of an object (a text, work of art, social action, utterances of another speaker, etc.) (Dictionary of Qualitative Inquiry, 2nd ed..) ]
Hermissenda D049870 [A genus of marine sea slugs in the family Glaucidae, superorder GASTROPODA, found on the Pacific coast of North America. They are used in behavioral and neurological laboratory studies. ]
Hernandiaceae D049935 [A plant family of the order Laurales, subclass Magnoliidae, class Magnoliopsida. Members contain cytotoxic furofuran LIGNANS and isoquinoline ALKALOIDS. ]
Hernia D006547 [An intestinal HERNIA. , Protrusion of tissue, structure, or part of an organ through the bone, muscular tissue, or the membrane by which it is normally contained. Hernia may involve tissues such as the ABDOMINAL WALL or the respiratory DIAPHRAGM. Hernias may be internal, external, congenital, or acquired. ]