UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM - Terms starting with ‘R’

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UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM

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A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

H H+ H1 HA HB HC HD HE HF HG HH HI HK HL HM HN HO HP HQ HR HS HT HU HV HX HY HZ

HEA HEB HEC HED HEE HEF HEI HEL HEM HEN HEP HER HES HET HEU HEV HEX HEY

selected terms: 104

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1. HER-2-neu peptide vaccine/Montanide ISA-51 (UMLS (NCI) C0879332) =Therapeutic or Preventive Procedure	51. HERNIA NEC (UMLS (ICD9CM) C0019275) =Disease or Syndrome; Anatomical Abnormality
2. HER-2-Neu Peptide Vaccine/Sargramostim (UMLS (NCI) C0879358) =Therapeutic or Preventive Procedure ;	52. HERNIA OF ABDOMINAL CAVITY [A protrusion of abdominal structures through the retaining ABDOMINAL WALL. It involves two parts: an opening in the abdominal wall, and a hernia sac consisting of PERITONEUM and abdominal contents. Abdominal hernias include groin hernia (HERNIA, FEMORAL; HERNIA, INGUINAL) and VENTRAL HERNIA. ( MSH )] (UMLS (ICD9CM) C0178282) =Disease or Syndrome; Anatomical Abnormality
3. HER-2/neu Helper-Peptide Vaccine [A cancer vaccine comprised of peptides derived from the extracellular domain of the tumor-associated antigen Her-2/neu with potential antineoplastic activity. HER-2/neu peptide vaccine may induce antibodies with anti-tumor activity and may also elicit a specific CD8 T-cell response against specific tumor cell types. (NCI04) ( NCI )] (UMLS (NCI) C0879250) HER-2/neu Peptide Vaccine; HER-2-Neu Peptide Vaccine =Amino Acid, Peptide, or Protein; Pharmacologic Substance; Immunologic Factor	53. Hernia of other specified sites, with gangrene [ ] (UMLS (ICD9CM) C0156125) =Acquired Abnormality; Disease or Syndrome
4. herbal medicine [The study of medicines derived from botanical sources. ( MSH )] (UMLS (CSP) C1533719) =Biomedical Occupation or Discipline; ;	54. Hernia of other specified sites, with obstruction [ ] (UMLS (ICD9CM) C0156139) =Acquired Abnormality; Disease or Syndrome
5. herbal tea [ ] (UMLS (CSP) C0019233) =Food ;	55. Hernia of unspecified site, with gangrene (UMLS (ICD9CM) C0267667) =Acquired Abnormality; Disease or Syndrome
6. herbicide [agent used to destroy unwanted vegetation. ( CSP )] (UMLS (NCI) C0019236) =Hazardous or Poisonous Substance ; =pesticide; =paraquat; 2,4,D/2,4,5,T;	56. Hernia of unspecified site, with obstruction [ ] (UMLS (ICD9CM) C0156140) =Disease or Syndrome ;
7. HERED CHOROID ATROPH NOS [ ] (UMLS (ICD9CM) C0154893) =Disease or Syndrome	57. Hernia with Obstruction without mention of Gangrene (UMLS (NCI) C1333995) =Anatomical Abnormality ;
8. HERED HEMOLYTIC ANEM NEC [ ] (UMLS (ICD9CM) C0154296) =Disease or Syndrome	58. herniated disk [ ] (UMLS (CSP) C0242362) =Disease or Syndrome ;
9. HERED PERIPH NEUROPATHY [ ] (UMLS (ICD9CM) C0392553) =Disease or Syndrome ;	59. Herniogram (UMLS (HL7) C1548857) =Health Care Activity =Consent Type;
10. HERED PROG MUSC DYSTRPHY [general term for a group of inherited disorders which are characterized by progressive degeneration of skeletal muscles. ( CSP )] (UMLS (ICD9CM) C0026850) =Congenital Abnormality; Disease or Syndrome =Genetic Condition; muscle disorder; Heredodegenerative Disorders, Nervous System; Muscular Disorders, Atrophic =Duchenne muscular dystrophy; myotonia atrophica; Duchenne muscular dystrophy; myotonia atrophica; facioscapulohumeral muscular dystrophy; Muscular Dystrophy, Emery-Dreifuss	60. Heroin Addiction [Strong dependence, both physiological and emotional, upon heroin. ( MSH )] (UMLS (NCI) C0019337) =Mental or Behavioral Dysfunction ; =Opioid-Related Disorders;
11. HERED RETIN DYSTRPHY NOS [ ] (UMLS (ICD9CM) C0154860) =Disease or Syndrome	61. heron hepatitis B virus [ ] (UMLS (CSP) C0598335) =Virus
12. HERED SENSORY NEUROPATHY [group of peripheral nervous system hereditary disorders with varying course, symptoms, neuropathology, and genetics, but characterized by degeneration of peripheral nerves, and clinically by loss of sensation. ( CSP )] (UMLS (ICD9CM) C0699739) =Disease or Syndrome =Peripheral Sensory Neuropathy; hereditary peripheral nervous system disorder	62. HERPANGINA (UMLS (ICD9CM) C0019338) =Disease or Syndrome ; =Coxsackievirus Infections;
13. HERED SPASTIC PARAPLEGIA [A group of inherited diseases that share similar phenotypes but are genetically diverse. Different genetic loci for autosomal recessive, autosomal dominant, and x-linked forms of hereditary spastic paraplegia have been identified. Clinically, patients present with slowly progressive distal limb weakness and lower extremity spasticity. Peripheral sensory neurons may be affected in the later stages of the disease. (J Neurol Neurosurg Psychiatry 1998 Jan;64(1):61-6; Curr Opin Neurol 1997 Aug;10(4):313-8) ( MSH )] (UMLS (ICD9CM) C0037773) =Disease or Syndrome ; =Hereditary Motor and Sensory Neuropathies;	63. Herpes [Any inflammatory skin disease caused by a herpesvirus and characterized by the formation of small vesicles in clusters. ( NCI )] (UMLS (NCI) C0019340) =Disease or Syndrome ;
14. HEREDIT HEMORR TELANGIEC [An autosomal dominant vascular anomaly characterized by telangiectases of the skin and mucous membranes and by recurrent gastrointestinal bleeding. This disorder is caused by mutations of a gene (on chromosome 9q3) which encodes endoglin, a membrane glycoprotein that binds TRANSFORMING GROWTH FACTOR BETA. ( MSH )] (UMLS (ICD9CM) C0039445) =Disease or Syndrome ; =telangiectasia; Vascular Hemostatic Disorders	64. herpes 2 [ ] (UMLS (CSP) C0598514) =Disease or Syndrome ;
15. HEREDIT TOOTH STRUCT NEC [ ] (UMLS (ICD9CM) C0868848) Hereditary disturbances in tooth structure, not elsewhere classified =Congenital Abnormality	65. Herpes Esophagitis (UMLS (NCI) C0238112) =Disease or Syndrome ;
16. hereditary [(ha-RED-ih-tair-ee) Transmitted from parent to child by information contained in the genes. ( NCI )] (UMLS (NCI) C0439660) =Functional Concept	66. Herpes genitalis (UMLS (ICPC) C0497572) (Herpes genitalis; HERPES GENITALA; Herpes Genitalis; Herpes genitalis; GENITAALIHERPES; Herpes genital; Herpes genitalis; (108); herpes genitalis; Herpes genitale; GENITAL HERPES + a60; Herpes genital; Herpes genital; GENITAL HERPES) Herpes genitalis in women =Disease or Syndrome =FEMALE GENITAL SYSTEM (INCLUDING BREAST); Diagnosis/Diseases Component ◊ (UMLS (ICPC) C0497579) (Herpes genitalis; HERPES GENITALA; Herpes genitalis; Herpes genitalis; HERPES GENITALIS; Herpes genital; Herpes genitalis; (108); herpes genitalis; Herpes genitale; GENITAL HERPES + a60; Herpes genital; Herpes genital; GENITAL HERPES) Herpes genitalis in men Disease or Syndrome Diagnosis/Diseases Component; Body System, Reproductive, Male
17. HEREDITARY AND DEGENERATIVE DISEASES OF THE CENTRAL NERVOUS SYSTEM (UMLS (ICD9CM) C1444208) =Disease or Syndrome ;	67. Herpes simplex [infection caused by the herpes simplex virus; affects the skin and nervous system; produces small temporary (but sometimes painful) blisters on the skin and mucous membranes.(CSP)] (UMLS (ICPC) C0019348) (Herpes simplex; HERPES SINPLEXA( ESKL. BEGIA F85; GENITALA X90, Y72); Herpes simplex (ex F85 X90 Y72); Herpes simplex (ex F85 X90 Y72); HERPES SIMPLEX (PL F85 X90 Y72); Herpes simplex (SF F85 X90 Y72); Herpes Simplex (ex F85 X90 Y72); herpes simpleks; herpes simplex (kiv.F85,X90,Y72); Herpes simplex(escl F85 X90 Y72); HERPES SIMPLEX EKS F85 X90 Y75; Herpes simplex (excl F85 X90 Y72) ; Herpes simple (ex F85 X90 Y72); HERPES SIMPLEX (EXKL F85 X90 Y72)) Herpes simplex (excl F85 X90 Y72); Herpes simplex (excluding F85 X90 Y72) =Disease or Syndrome ; =Herpesviridae disease; opportunistic infection; Skin Diseases, Viral; Diagnosis/Diseases Component; Integument; =Genital Herpes; Keratitis, Herpetic; Genital Herpes; cold sore; Keratitis, Herpetic; Kaposi Varicelliform Eruption; Stomatitis, Herpetic
18. Hereditary and idiopathic peripheral neuropathy [ ] (UMLS (ICD9CM) C0154754) =Disease or Syndrome	68. herpes simplex 2 [herpes simplex virus, type 2 vaccine ( HL7V3.0 )] (UMLS (HL7) C1548481) =Pharmacologic Substance; Immunologic Factor ; =Vaccines administered (code = CVX)(parenteral, unless oral is noted); VaccineType
19. hereditary ataxia [ ] (UMLS (CSP) C0004138) =Disease or Syndrome	69. Herpes Simplex Dermatitis (UMLS (NCI) C0854331) =Disease or Syndrome
20. Hereditary Benign Intraepithelial Dyskeratosis (UMLS (NCI) C0265966) =Disease or Syndrome ;	70. Herpes simplex dermatitis of eyelid [ ] (UMLS (ICD9CM) C0153037) =Disease or Syndrome
21. hereditary carnitine deficiency lipid storage myopathy [ ] (UMLS (CSP) C0598584) =Disease or Syndrome	71. HERPES SIMPLEX EYE NEC [ ] (UMLS (ICD9CM) C0153040) =Disease or Syndrome
22. hereditary carnitine deficiency myopathy [rare genetic carnitine metabolic disorder that causes extreme muscle weakness; carnitine functions in the body as a carrier of fatty acids to the energy centers in muscles (mitochondria). ( CSP )] (UMLS (CSP) C0596692) =Disease or Syndrome ; =inborn biological transport disorder;	72. HERPES SIMPLEX EYE NOS [ ] (UMLS (ICD9CM) C0153036) =Disease or Syndrome
23. hereditary cerebellar degeneration [ ] (UMLS (CSP) C0270752) =Disease or Syndrome	73. HERPES SIMPLEX MYELITIS [ ] (UMLS (ICD9CM) C1719298) =Disease or Syndrome
24. hereditary ceroid lipofuscinosis [inherited degenerative disease characterized by neuronal cytoplasmic inclusions which stain positively for ceroid and lipofuscin. ( CSP )] (UMLS (CSP) C0027877) =Disease or Syndrome ; =inborn lipid storage disorder; Arrieration mentale; Heredodegenerative Disorders, Nervous System;	74. HERPES SIMPLEX NOS [ ] (UMLS (ICD9CM) C0392646) =Disease or Syndrome
25. hereditary chorea [ ] (UMLS (CSP) C0699731) =Disease or Syndrome	75. herpes simplex virus [HSV is a nuclear replicating, icosahedral, enveloped DNA virus. The HSV envelope contains at least 8 glycoproteins. The matrix or tegument which contacts both the envelope and the capsid contains at least 15-20 proteins. There are two types of HSV - Type 1 and Type 2. The Type 1 virus causes cold sores. Most people get Type 1 infections during infancy or childhood. The Type 2 virus causes genital sores. Most people get Type 2 infections following sexual contact with an infected person. ( NCI )] (UMLS (CSP) C0206558) =Virus
26. Hereditary Clear Cell Renal Cell Carcinoma [A manifestation of von Hippel-Lindau disease or other familial renal cell cancer syndromes that present as a malignant epithelial neoplasm of the kidney. It is characterized by the presence of lipid-containing clear cells within a vascular network. The tumor usually is bilateral and polycentric, and metastasizes to unusual sites. Late metastasis is common. ( NCI )] (UMLS (NCI) C1333985) Hereditary Conventional (Clear Cell) Renal Cell Carcinoma =Neoplastic Process ;	76. herpes simplex virus 1 [causes cold sores in humans, especially in young children. ( CSP )] (UMLS (CSP) C0206679) =Virus ; =Alphaherpesvirinae;
27. hereditary coproporphyria porphyria [An autosomal dominant porphyria that is due to a deficiency of COPROPORPHYRINOGEN OXIDASE in the LIVER, the sixth enzyme in the 8-enzyme biosynthetic pathway of HEME. Clinical features include both neurological symptoms and cutaneous lesions. Patients excrete increased levels of porphyrin precursors, 5-AMINOLEVULINATE and COPROPORPHYRINS. ( MSH )] (UMLS (CSP) C0162531) =Disease or Syndrome	77. herpes simplex virus 2 [similiar to herpes simplex 1 except that it is usually transmitted sexually; causes genital lesions and may cause carcinoma of the cervix. ( CSP )] (UMLS (CSP) C0019351) =Virus ; =Alphaherpesvirinae;
28. Hereditary disease in family possibly affecting fetus, affecting management of mother [ ] (UMLS (ICD9CM) C0157072) =Disease or Syndrome ;	78. Herpes Simplex Virus Thymidine Kinase Gene [Herpes simplex virus thymidine kinase (HSV-Tk) gene encodes thymidine kinase protein, which is important for herpes simplex virus infection. The TK gene and promoter are widely used in genetic research because of the easily selectable phenotype. ( NCI )] (UMLS (NCI) C1333929) HSV-Tk; HSV-Tk Gene =Gene or Genome ;
29. HEREDITARY EDEMA OF LEGS [ ] (UMLS (ICD9CM) C1313885) =Disease or Syndrome; ;	79. Herpes simplex visceral (UMLS (ICD9CM) C0019359) =Disease or Syndrome ;
30. hereditary factor VII deficiency [ ] (UMLS (CSP) C0272320) =Disease or Syndrome	80. herpes virus [family of enveloped DNA viruses; occur in man, cold-blooded vertebrates, and invertebrates; some may induce neoplasia; transmission is usually by contact but it can occur by other routes. ( CSP )] (UMLS (NCI) C0019369) =Virus =DNA virus; =Herpesvirus saimiri; HBLV; Alphaherpesvirinae; Betaherpesvirinae; Gammaherpesvirinae
31. hereditary hemochromatosis [disorder due to the deposition of hemosiderin in the parenchymal cells, causing tissue damage and dysfunction of the liver, pancreas, heart, and pituitary; full development of the disease in women is restricted by menstruation, pregnancy, and lower dietary intake of iron; an autosomal recessive disorder of metabolism associated with a gene tightly linked to the A locus of the HLA complex on chromosome 6. ( CSP )] (UMLS (CSP) C0392514) =Disease or Syndrome ; =inborn metal metabolism disorder;	81. Herpes zoster [acute infectious, usually self-limited, disease believed to represent activation of latent varicella zoster virus in those who have been rendered partially immune after a previous attack of chickenpox; it involves the sensory ganglia and their areas of innervation and is characterized by severe neuralgic pain along the distribution of the affected nerve and crops of clustered vesicles over the area.(CSP)] (UMLS (ICPC) C0019360) (Herpes zoster; ZOSTER HERPESA; Herpes Zoster; Herpes zoster; VYORUUSU; Herpes zoster; Herpes Zoster; shalbeket xogeret; herpes zooster; Herpes zoster; HERPES ZOSTER; Herpes zoster; Herpes zoster; HERPES ZOSTER/BALTROS) Herpes zoster =Disease or Syndrome ; =Herpesviridae disease; Diagnosis/Diseases Component; Integument; =GENICULATE HERPES ZOSTER; Herpes Zoster Ophthalmicus;
32. Hereditary hemolytic anemias [includes hereditary erythrocyte membrane defects, enzyme deficiencies, hemoglobin abnormalities, stem cell defects (paroxysmal nocturnal hemoglobinuria), and alloimmune (Rh) disease of newborn.(CSP)] (UMLS (ICPC) C0002881) (Hereditary hemolytic anemias; ANEMIA HEMOLITIKOA; Medfodt haemolytisk anaemi; Erfelijke hemolytische anemie; PERINNOLLISET HEMOLYYTTISET ANEMIAT; Anemies hemolytiques hereditaires; Hereditaere Haemolytische Anaemie; (108); orokletes haemolytikus anaemiak; Anemie emolitiche ereditarie; MEDFODTE HEMOLYTISKE ANEMIER; Anemias hemoliticas hereditarias; Anemias hemoliticas hereditarias; ARFTLIGA HEMOLYTISKA ANEMIER) =Disease or Syndrome	82. Herpes Zoster Dermatitis (UMLS (NCI) C0854330) =Disease or Syndrome
33. hereditary hyperbilirubinemia [inborn errors of bilirubin metabolism resulting in excessive amounts of bilirubin in the circulating blood, either because of increased bilirubin production or because of delayed clearance of bilirubin from the blood. ( CSP )] (UMLS (CSP) C0020435) =Disease or Syndrome =hyperbilirubinemia; Congenital Metabolic Disorder; Congenital anomalies of the integument; =Crigler Najjar syndrome; congenital nonhemolytic jaundice	83. Herpes zoster dermatitis of eyelid (UMLS (ICD9CM) C0019362) =Disease or Syndrome ;
34. hereditary hyperglycemic obesity [inherited abnormal increase of glucose in the blood resulting in an increase in body weight beyond skeletal and physical standards as the result of an excessive accumulation of fat in the body. ( CSP )] (UMLS (CSP) C0596693) =Pathologic Function ; =Carbohydrate Metabolism, Inborn Errors;	84. HERPES ZOSTER MENINGITIS (UMLS (ICD9CM) C0700503) =Disease or Syndrome
35. Hereditary Nephritis [A group of inherited conditions characterized initially by HEMATURIA and slowly progressing to RENAL INSUFFICIENCY. The most common form is the Alport syndrome (hereditary nephritis with HEARING LOSS) which is caused by mutations in genes for TYPE IV COLLAGEN and defective GLOMERULAR BASEMENT MEMBRANE. ( MSH )] (UMLS (NCI) C0027706) =Disease or Syndrome =nephritis; Congenital Genitourinary Abnormality	85. HERPES ZOSTER MYELITIS [ ] (UMLS (ICD9CM) C1719297) =Disease or Syndrome
36. hereditary neuropathy [ ] (UMLS (CSP) C0598589) =Disease or Syndrome	86. HERPES ZOSTER NOS (UMLS (ICD9CM) C0019366) =Disease or Syndrome ;
37. HEREDITARY OPTIC ATROPHY [Hereditary conditions that feature progressive visual loss in association with optic atrophy. Relatively common forms include autosomal dominant optic atrophy (OPTIC ATROPHY, AUTOSOMAL DOMINANT) and Leber hereditary optic atrophy (OPTIC ATROPHY, HEREDITARY, LEBER). ( MSH )] (UMLS (ICD9CM) C0029125) =Congenital Abnormality; Disease or Syndrome =Eye Diseases, Hereditary; optic atrophy; Heredodegenerative Disorders, Nervous System;	87. HERPES ZOSTER OF EYE NEC (UMLS (ICD9CM) C0795698) Herpes zoster with other ophthalmic complications; =Disease or Syndrome ;
38. hereditary peripheral nervous system disorder [inherited diseases of the peripheral nerves external to the brain and spinal cord, which includes diseases of the nerve roots, ganglia, plexi, autonomic nerves, sensory nerves, and motor nerves. ( CSP )] (UMLS (CSP) C0596694) =Disease or Syndrome ; =Genetic Condition; DISORDERS OF THE PERIPHERAL NERVOUS SYSTEM =Hereditary Motor and Sensory Neuropathies; HERED SENSORY NEUROPATHY	88. Herpesviridae disease [infection by a member of the Herpesviridae family, a family of enveloped, linear, double-stranded DNA viruses; occurs in a wide variety of animals. ( CSP )] (UMLS (CSP) C0019372) =Disease or Syndrome =DNA Virus Infections; Infection, Viral =abaabuot ruax; Herpes simple (ex F85 X90 Y72); herpes zona; fowl paralysis; Lucke renal adenocarcinoma; abaabuot ruax; CYTOMEGALOVIRAL DISEASE; Herpes simple (ex F85 X90 Y72); herpes zona; Infectious Bovine Rhinotracheitis; Malignant Catarrh; fowl paralysis; Pseudorabies; HHV 8; EBV Infection; Encephalitis, Varicella Zoster; Encephalitis, Herpes Simplex; ANSIKTSFORLAMNING/BELLS PARES; Roseolovirus Infections
39. hereditary persistence of fetal hemoglobin [ ] (UMLS (CSP) C0019025) =Disease or Syndrome ;	89. Herpesviridae vaccine [vaccines or candidate vaccines used to prevent infection by any virus from the family Herpesviridae. ( CSP )] (UMLS (CSP) C0596696) =Immunologic Factor ; =viral vaccine;
40. hereditary protein C deficiency [ ] (UMLS (CSP) C0598221) =Disease or Syndrome ;	90. Herpesvirus ateles [ ] (UMLS (CSP) C0206563) =Virus
41. Hereditary Sideroblastic Anemia (UMLS (NCI) C0221018) =Disease or Syndrome	91. Herpesvirus saimiri [produces malignant lymphomata in marmosets and owl monkeys with lymphocytosis and reticular cell invasion of the viscera. ( CSP )] (UMLS (CSP) C0019376) =Virus =herpes virus;
42. hereditary spherocytosis [autosomal dominant trait marked by splenomegaly, jaundice, and fragile, spheroid erythrocytes which are prematurely cleared by the spleen; anemia is usually mild; treatment is splenectomy. ( CSP )] (UMLS (CSP) C0037889) =Disease or Syndrome ; =ANEMIA HEMOLITIKOA; Genetic Condition	92. Herpesvirus suis [A species of VARICELLOVIRUS producing a respiratory infection (PSEUDORABIES) in swine, its natural host. It also produces an usually fatal ENCEPHALOMYELITIS in cattle, sheep, dogs, cats, foxes, and mink. ( MSH )] (UMLS (CSP) C0033840) =Virus
43. heredity [The transmission of traits encoded in GENES from parent to offspring. ( MSH )] (UMLS (CSP) C0019266) =Molecular Function ;	93. HERPETIC ENCEPHALITIS (UMLS (ICD9CM) C0019385) =Disease or Syndrome
44. heredopathia atactica polyneuritiformis [autosomal recessive disorder of lipid metabolism in which deficiency of phytanic acid alpha-hydroxylase results in accumulation of phytanic acid; manifested chiefly by chronic polyneuritis, retinitis pigmentosa, cerebellar ataxia and elevation of protein in cerebrospinal fluid. ( CSP )] (UMLS (CSP) C0034960) =Disease or Syndrome ; =inborn lipid storage disorder; Hereditary Motor and Sensory Neuropathies; Polyneuropathies;	94. Herpetic Gastritis (UMLS (NCI) C1333996) =Disease or Syndrome ;
45. heregulin [contains an immunoglobulin-like domain that may function to advance malignancy and in cell-cell homing and adhesion, which are important events in cancer metastasis. ( CSP )] (UMLS (CSP) C0597718) =Amino Acid, Peptide, or Protein; Biologically Active Substance =binding protein;	95. HERPETIC GINGIVOSTOMAT [ ] (UMLS (ICD9CM) C0376379) =Disease or Syndrome
46. Heregulin Receptor [Comprised of the erbB2, erbB3, and erbB4 proteins. These proteins form homo and heterodimers, which complicates the assignment of specificities: it is known that erbB2 homodimer do not bind heregulin, but erbB2/erbB3 heterodimers do. ( NCI )] (UMLS (NCI) C1334952) Neuregulin Receptor =Amino Acid, Peptide, or Protein; Receptor	96. HERPETIC INFECT OF PENIS [ ] (UMLS (ICD9CM) C0153034) =Disease or Syndrome
47. heritable connective tissue disorder [ ] (UMLS (CSP) C0410787) =Disease or Syndrome	97. HERPETIC SEPTICEMIA [ ] (UMLS (ICD9CM) C0153041) =Disease or Syndrome
48. hermaphroditism [ambiguous external genitalia with both testicular and ovarian tissue present in the same individual. ( CSP )] (UMLS (CSP) C0019269) =Congenital Abnormality; Disease or Syndrome =sex differentiation disorder; congenital reproductive system disorder; sex development disorder; =pseudohermaphroditism	98. HERPETIC ULCER OF VULVA [ ] (UMLS (ICD9CM) C0153033) =Disease or Syndrome
49. Hermissenda [soft-bodied shell-less gastropods with simple nervous systems; used in neurobiological studies of learning and memory. ( CSP )] (UMLS (CSP) C0596695) =Invertebrate ; =Gastropoda;	99. HERPETIC VULVOVAGINITIS (UMLS (ICD9CM) C0019386) =Disease or Syndrome
50. hernia [protrusion of a loop or knuckle of an organ or tissue through an abnormal opening. ( CSP )] (UMLS (CSP) C0019270) =Disease or Syndrome; Anatomical Abnormality =Disease; Gastrointestinal Diseases; Pathological Conditions, Anatomical; =Diaphragmatic Hernia; Femoral Hernia; beka mifsaati axer; Hernia, Obturator; Hernia, Umbilical; Hernia, Ventral; Gastroschisis	100. HERPETIC WHITLOW [ ] (UMLS (ICD9CM) C0153042) =Disease or Syndrome

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