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ABETALIPOPROTEINAEMIA ABSCESS ABSCESS BREAST ABSCESS LIVER ACARIASIS ACHONDROPLASIA ACID MALTASE DEFICIENCY ACROMEGALY ACTINOMYCOSIS ACTIVATED PROTEIN C RESISTANCE ADDISONS DISEASE ADDISONS DISEASE AUTOIMMUNE ADENOSINE DEAMINASE DEFICIENCY ADENYLATE KINASE DEFICIENCY ADENYLOSUCCINASE DEFICIENCY ADENYLSUCCINATE LYASE DEFICIENCY ADRENAL DISEASE AUTOIMMUNE ADRENOCORTICAL HYPERFUNCTION ADRENOCORTICAL INSUFFICIENCY ADRENOLEUCODYSTROPHY AGAMMAGLOBULINAEMIA ALCOHOL ABUSE ALLERGY ALLERGY DUST MITE ALPHA-1-ANTITRYPSIN DEFICIENCY ALVEOLAR RHABDOMYOSARCOMA ALZHEIMERS DISEASE AMINOACIDURIAS AMOEBIASIS AMYLOIDOSIS AMYLOIDOSIS RENAL FAMILIAL AMYOTROPHIC LATERAL SCLEROSIS (ALS) ANAEMIA ANAEMIA HAEMOLYTIC ANAEMIA HEREDITARY ANAEMIA HYPOCHROMIC ANAEMIA IRON DEFICIENCY ANAEMIA MEGALOBLASTIC ANAEMIA OBSCURE ANAEMIA OF CHRONIC DISEASE ANAEMIA PERNICIOUS ANAEMIA SICKLE CELL ANAEMIA SIDEROBLASTIC ANAPHYLAXIS ANGELMAN SYNDROME ANGIODYSPLASIA ANAEMIA ANGIOEDEMA ACQUIRED ANGIOEDEMA HEREDITARY ANGIOSTRONGYLIASIS ANGULAR STOMATITIS ANHYDROTIC ECTODERMAL DYSPLASIA ANKYLOSING SPONDYLITIS ANOREXIA NERVOSA ANTI CHOLINESTERASE EXPOSURE ANTI THROMBIN III DEFICIENCY ANTICARDIOLIPIN SYNDROME ANTIPHOSPHOLIPID SYNDROME AORTIC ANEURYSMS FAMILIAL APERT SYNDROME APLASIAS APLASTIC ANAEMIA APNOEA ASSOCIATED WITH ANAESTHETIC APRT DEFICIENCY ARGININO-SUCCINIC ACID LYASE DEFICIENCY ARGINOSUCCINATE LYASE DEFICIENCY ARGYRIA (SILVER POISONING) AROMATIC AMINO ACID DECARBOXYLASE DEFICIENCY ARTHRITIS - POLYARTHRITIS ARTHRITIS REACTIVE ARTHRITIS RHEUMATOID ARTHRITIS VIRAL ARTHROPATHY CRYSTAL ASPARTYLGLUCOSAMINURIA ASPERGILLOSIS ASTHMA ASTHMA / CHRONIC AIR FLOW LIMITATION (CAL) ASTHMA EXCERCISE INDUCED ATAXIA TELANGECTASIA ATOPY ATYPICAL TERATOID RHABDOID TUMOUR AUTOIMMUNE DISEASE AUTOIMMUNE DISEASES OF THE CNS AUTOIMMUNE THYROID DISEASE AUTOSOMAL DOMINANT SPASTIC PARAPLEGIA BACTERIAL OVERGROWTH BANNAYAN-RILEY-RUVALCABA SYNDROME BARTTERS SYNDROME BATTEN DISEASE BECKERS DISEASE BECKWITH WIEDEMANN SYNDROME BERI BERI BETA CELL DYSFUNCTION BILHARZIASIS BIOTINIDASE DEFICIENCY BIPOLAR DISORDERS BIRD FANCIERS DISEASE BLASTOMYCOSIS BLOOMS SYNDROME BONE MARROW TRANSPLANT BONE METABOLISM BONE RESORPTION BORRELIOSIS BOTULISM BRONCHIOLITIS BRUCELLOSIS BRUTONS X-LINKED HYPOGAMMAGLOBULINAEMIA BULLOUS PHEMPHIGOID CADASIL CALCULUS RENAL CAMPYLOBACTERIOSIS CANAVANS DISEASE CANCER CANCER OF LUNG ( SMALL CELL ) CANCER ADRENAL CANCER BONE CANCER BREAST CANCER CERVICAL CANCER COLORECTAL CANCER ENDOCRINE CANCER ENDOMETRIAL CANCER HAEM MALIGNANCY CANCER HAEMATOLOGICAL CANCER HAEMATOMA CANCER HYPOGLYCAEMIA CANCER IMMUNOLOGICAL CANCER LIVER CANCER METASTATIC CANCER NEURAL CREST CANCER NEUROENDOCRINE CANCER OVARIAN CANCER PANCREATIC CANCER PITUITARY CANCER PRORENIN PRODUCING CANCER PROSTATE CANCER STOMACH CANCER T CELL CANCER TESTICULAR CANCER THYROID CANCER THYROID MEDULLARY CANCER TROPHOBLASTIC CANDIDAEMIA CANDIDIASIS CARBAMYL PHOSPHATE SYNTHETASE DEFICIENCY CARBON MONOXIDE POISONING CARCINOID SYNDROME CARDIAC ARRHYTHMIAS CARDIAC FAILURE CARDIAC FAILURE CONGESTIVE CARDIOMYOPATHY CARDIOVASCULAR DISEASE CARNITINE DEFICIENCY CARNITINE PALMITOYL TRANSFERASE I CARNITINE PALMITOYL TRANSFERASE I DEFICIENCY CARNITINE PALMITOYL TRANSFERASE II DEFICIENCY CARNITINE PALMITYL TRANSFERASE DEFICIENCY TYPE II CARNITINE TRANSPORTER DEFECT CAROTENAEMIA CAT SCRATCH DISEASE CATALASE DEFICIENCY CBAVD (CONGENITAL BILATERAL ABSENCE OF THE VAS DEFERENS) CDA TYPE II CDG TYPE IA CDG TYPE IB CDRI DISEASE CENTRAL CORE DISEASE CERAMIDASE DEFICIENCY CEREBROTENDINOUS XANTHOMATOSIS (CTX) CEREBROVASCULAR DISEASE CEROID LIPOFUSCINOSIS NEURONAL 1 CEROID LIPOFUSCINOSIS NEURONAL 1 CEROID LIPOFUSCINOSIS NEURONAL 2 CERVICITIS CHAGAS DISEASE CHARCOT-MARIE-TOOTH DISEASE CHARCOT-MARIE-TOOTH NEUROPATHY - TYPE 2A CHICKEN POX CHLAMYDIA CHOLANGITIS CHOLELITHIASIS CHOLERA CHOLESTASIS CHOLESTASIS IN PREGNANCY CHOLESTERYL ESTER STORAGE DISEASE CHONDROPLASIA PUNCTATA 2 CHOTZEN SYNDROME CHRISTMAS DISEASE CHRONIC AIR FLOW LIMITATION (CAL) CHRONIC PROGRESSIVE EXTERNAL OPTHALMOPLEGIA (CPEO) CIDP (CHRONIC INFLAMMATORY DEMYELINATING POLYNEUROPATHY) CIRRHOSIS CIRRHOSIS JUVENILE CIRRHOSIS PRIMARY BILIARY CITRULLINAEMIA CLONAL T CELL DISEASE COAGULATION FACTOR DEFICIENCY (EXTRINSIC PATHWAY) COAGULATION FACTOR DEFICIENCY (INTRINSIC PATHWAY) COCCIDIOIDOMYCOSIS COELIAC DISEASE COLD AGGLUTININ DISEASE (CAD) COLITIS COMBINED PITUITARY HORMONE DEFICIENCY COMBINED PITUITARY HORMONE DEFICIENCY (CPHD) COMPLEMENT DEFICIENCY CONDYLOMATA ACCUMINATA (GENITAL WARTS) CONGENITAL ABSENCE OF VAS (CAV) CONGENITAL ADRENAL HYPERPLASIA (CAH) CONGENITAL DISORDER OF GLYCOSYLATION TYPE 1a CONGENITAL DISORDERS OF GLYCOSYLATION !A and 1B CONGENITAL DISORDERS OF GLYCOSYLATION TYPE IA CONGENITAL DISORDERS OF GLYCOSYLATION TYPE IB CONGENITAL HYPOMYELINATING NEUROPATHY CONGENITAL NON-SPHEROCYTIC HAEMOLYTIC ANAEMIA (CNSHA) CONJUNCTIVITIS CONNECTIVE TISSUE DISEASE CONNS SYNDROME CONRADI-HUNERMANN-HAPPLE SYNDROME X-LINKED DOMINANT CORPUS LUTEAL INSUFFICIENCY COWDENS SYNDROME CRANIOSYNOSTOSIS CREUTZFELD-JACOB DISEASE (CJD) CROHNS DISEASE CRYPTOCOCCOSIS CRYPTOSPORIDIOSIS CURRARINOS SYNDROME CUSHINGS SYNDROME CYSTIC FIBROSIS CYSTICERCOSIS CYSTINOSIS CYSTINURIA CYSTITIS CYSTITIS HAEMORRHAGIC D VARIANTS DBIFUNCTIONAL PROTEIN DEFICIENC D-BIFUNCTIONAL PROTEIN DEFICIENCY DEAFNESS DEBRANCHER ENZYME DEFICENCY DEBRANCHER ENZYME DEFICIENCY DEEP VENOUS THROMBOSIS (DVT) DENGUE FEVER DENTATO RUBRAL PALLIDOLUYSIAN ATROPHY (DRPLA) DENTATORUBRAL-PALLIDOLUYSIAN ATYOPHY (DRPLA) DERMATITIS HERPETIFORMIS DESMOPLASTIC SMALL ROUND CELL TUMOUR DEVELOPMENTAL DELAY DIABETES DIABETES MELLITUS DIABETES MELLITUS TYPE I DIABETES INSIPIDUS DIABETES MELLITUS DIABETES MELLITUS TYPE I DIABETIC KETOACIDOSIS DIABETIC NEPHROPATHY DIALYSIS DIARRHOEA DIHYDROPTERIDINE REDUCTASE (DHPR) DEFICIENCY DIPHTHERIA DIPHTHERIA VACCINATION DISSEMINATED INTRAVASCULAR COAGULATION (DIC) DOPA RESPONSIVE DYSTONIA DOWNS SYNDROME (TRISOMY 21) DRASH SYNDROME DRESSLERS SYNDROME DRUG INGESTION (eg. Aspirin, NSAIDs) DUBIN JOHNSON SYNDROME DUNCANS DISEASE DYSBETALIPOPROTEINAEMIA DYSFIBRINOGENAEMIA DYSLIPIDAEMIA DYSTONIA ECHINOCOCCOSIS EMPHYSEMA ENCEPHALITIS ENCEPHALITIS AUSTRALIAN ENCEPHALITIS JAPANESE ENCEPHALITIS KUNJIN ENCEPHALITIS MURRAY VALLEY ENCEPHALITIS UNKNOWN ORIGIN ENCEPHALOMYOCARDITIS ENCEPHALOPATHY HEPATIC ENCEPHALOPATHY MITOCHONDRIAL ENDOCARDIAL FIBROELASTOSIS TYPE 2 ENDOCARDIAL FIBROELASTOSIS X-LINKED ENDOCARDITIS ENTERITIS ENTEROBIASIS EPISODIC ATAXIA TYPE 2 EPSTEIN BARR VIRUS EQUINE MORBILLIVIRUS DISEASE ERYTHEMA INFECTIOSUM (FIFTH DISEASE) ERYTHROPOIETIN (EPO) MONITORING EWINGS SARCOMA EXANTHEM SUBITUM FABRY DISEASE FACTOR DEFICIENCY FACTOR V LEIDEN ABNORMALITY FAMILIAL ADENOMATOUS POLYPOSIS (FAP) FAMILIAL AMYLOIDOTIC POLYNEUROPATHY FAMILIAL DYSAUTONOMIA FAMILIAL GLUCOCORTICOID DEFICIENCY FAMILIAL GLUCOCORTICOID DEFICIENCY (FGD) FAMILIAL HEMIPLEGIC MIGRAINE FAMILIAL HYPERCHOLESTEROLAEMIA FAMILIAL MEDITERRANEAN FEVER FAMILIAL PARAGANGLIOMA FAMILIAL X-LINKED DISORDERS FANCONI ANAEMIA FANCONI SYNDROME FARBERS DISEASE FASCIOLIASIS FASCIOSCAPULOHUMERAL MUSCULAR DYSTROPHY FAT MALABSORPTION SYNDROME FATTY ACID OXIDATION DEFECTS FAVISM FETAL LUNG MATURITY FETO MATERNAL HAEMORRHAGE (FMH) FIBROSING ALVEOLITIS FIFTH DISEASE FILARIASIS BANCROFTIAN FOLATE DEFICIENCY FRAGILE X SYNDROME FRAGILE XA SYNDROME FRAGILE XE NON SPECIFIC XLMR (X-LINKED MENTAL RETARDATION) FRASIER SYNDROME FRIEDREICHS ATAXIA FRUCTOSE INTOLERANCE HEREDITARY FUCOSIDOSIS FUMARIC ACIDURIA GALACTOKINASE DEFICIENCY GALACTOSAEMIA GALACTOSIALIDOSIS GANGLIONEUROMA GANGLIOSIDOSIS GM1 GASTROENTERITIS GASTRO-OESOPHAGEAL REFLUX GAUCHER DISEASE GAUCHER DISEASE GAUCHERS DISEASE GERSTMAN STRAUSSLER SCHEINKER DISEASE (GSS) GIARDIASIS GILBERTS DISEASE GITLEMANS SYNDROME GLOMERULONEPHRITIS GLUCAGONOMA GLUCOSE INTOLERANCE GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY GLUCOSE-6-PHOSPHATE DEFICIENCY (G6PD) GLUTATHIONE SYNTHETASE DEFICIENCY GLYCOGEN STORAGE DISEASE 1a GLYCOGEN STORAGE DISEASE TYPE 5 GLYCOGEN STORAGE DISEASE TYPE 6 GLYCOGEN STORAGE DISEASE TYPE IA GLYCOGEN STORAGE DISEASE TYPE II GLYCOGEN STORAGE DISEASE TYPE IX GLYCOGEN STORAGE DISEASE TYPE V GLYCOGEN STORAGE DISEASE TYPE VI GLYCOGEN STORAGE DISORDER GLYCOGEN STORAGE DISORDER TYPE III GM2 GANGLIOSIDOSIS TYPE 1 GM2 GANGLIOSIDOSIS TYPE 2 GONORRHOEA GOODPASTURES SYNDROME GOUT GRANULOMATOUS AMOEBIC ENCEPHALITIS (GAE) GRANULOMATOUS DISEASE GRANULOMATOUS DISEASE CHRONIC GRAVES DISEASE GROWTH HORMONE DEFICIENCY GROWTH RETARDATION GTP-CH DEFICIENCY DOPA RESPONSIVE DYSTONIA GUILLAIN BARRE SYNDROME HAEMATEMASIS FETAL HAEMATOMA RETROPERITONEAL HAEMOCHROMATOSIS HAEMOGLOBINOPATHIES HAEMOLYSIS HAEMOLYSIS COMPLEMENT MEDIATED HAEMOLYSIS HEART VALVE HAEMOLYSIS INTRAVASCULAR HAEMOLYSIS OXIDATIVE HAEMOLYTIC DISEASE OF THE NEWBORN (HDN) HAEMOLYTIC PLUS BLEEDING HAEMOLYTIC URAEMIC SYNDROME (HUS) HAEMOPHILIA HAEMOPHILIA A HAEMOPHILIA B HAEMOPHILUS INFLUENZAE (HIB) HAEMOPHILUS INFLUENZAE VACCINATION HAEMORRHAGE SUBARACHNOID HAEMORRHAGIC CYSTITIS IN RENAL TRANSPLANT PATIENTS HAEMORRHAGIC FEVER HAEMORRHAGIC FEVER WITH RENAL SYNDROME HAEMORRHAGIC URAEMIC SYNDROME (HUS) HAND FOOT AND MOUTH DISEASE HANSENS DISEASE (LEPROSY) HARTNUPS DISEASE HASHIMOTOS THYROIDITIS HAYFEVER HEAPATITIS B HEART BLOCK CONGENITAL HEPARIN THERAPY HEPATITIS HEPATITIS A HEPATITIS AUTOIMMUNE HEPATITIS B HEPATITIS C HEPATITIS CHRONIC ACTIVE HEPATITIS D HEPATITIS E HEPATITIS G HEPATITIS GENERAL HEPATO - PULMONARY ABNORMALITIES HEPATOCELLULAR DISEASE HEREDITARY CEREBRAL HAEMORRHAGE WITH AMYLOIDOSIS HEREDITARY NONPOLYPOSIS COLON CANCER (HNPCC) HEREDITARY PERSISTENCE OF FETAL HAEMOGLOBIN (HPFH) HEREDITARY SENSORY NEUROPATHY HEREDITARY SPHEROCYTOSIS HERPES SIMPLEX HERPES ZOSTER (SHINGLES) HERS DISEASE HGPRT DEFICIENCY HIBERNIAN FEVER HIRSCHSPRUNGS DISEASE HIRSUITISM HIRSUTISM HIRSUTISM, VIRILISM HISTOPLASMOSIS HIV / AIDS HOMOCYSTINURIA HOOKWORM DISEASE HUNTER SYNDROME HUNTINGTONS DISEASE HURLER SYNDROME HYALINE MEMBRANE DISEASE OF NEWBORN HYDATID DISEASE HYDROPS FOETALIS HYDROXYLASE DEFICIENCY - 11-BETA HYPER/HYPOGAMMAGLOBULINAEMIA HYPERALDOSTERONISM HYPERALDOSTERONISM FAMILIAL HYPERALDOSTERONISM FAMILIAL AND SECONDARY HYPERAMMONAEMIAS GENETIC HYPERCALCAEMIA - CANCER RELATED HYPERCHOLESTEROLAEMIA HYPERCHOLESTEROLAEMIA (PRIMARY OR SECONDARY) HYPERCHOLESTEROLAEMIA FAMILIAL HYPERCHONDROPLASIA HYPEREOSINOPHILIC SYNDROME (HES) HYPERINSULINISM HYPERAMMONIA SYNDROME HYPERPARATHYROIDISM HYPERPROLACTINAEMIA HYPERTENSION HYPERTHYROIDISM HYPERTRIGLYCERIDAEMIA PRIMARY HYPOCAERULOPLASMINAEMIA HYPOCALCIURIA FAMILIAL HYPOCHONDROPLASIA HYPOFIBRINOGENAEMIA HYPOGONADISM IN MALES HYPOGONADISM MALE AND FEMALE HYPONATRAEMIA HYPOPHOSPHATASIA HYPOPITUITARISM HYPOTHYROIDISM HYPOTHYROIDISM CONGENITAL HYPOTHYROIDISM SECONDARY I CELL DISEASE ICHTHYOSIS X-LINKED IgA DEFICIENCY IgA DEFICIENCY SELECTIVE IMMUNODEFICIENCY SYNDROME INCONTINENTIA PIGMENTI INFANTILE BATTEN DISEASE INFANTILE NEURONAL CEROID LIPOFUSCINOSIS INFARCTION INTESTINAL INFECTION RECURRENT INFECTIOUS MONONUCLEOSIS (GLANDULAR FEVER) INFERTILITY INFERTILITY MALE INFLAMMATORY CONDITIONS INFLAMMATORY DISEASES CNS INSOMNIA FATA FALMILIAL INSULIN RESISTANCE INSULINOMA INTERSTITIAL LUNG DISEASE (ILD) IRON DEFICIENCY IRON OVERLOAD JANSKY-BIELSCHOWSKY DISEASE JUVENILE CEROID LIPOFUSCINOSIS NEURONAL 3 JUVENILE NEURONAL NEURONAL LIPOFUSCINOSIS KALA-AZAR KALLMANNS SYNDROME KARPOSIS SARCOMA KARTAGENERS SYNDROME KASHIN-BECK DISEASE KEARNS-SAYRE SYNDROME KENNEDYS DISEASE KERATITIS AMOEBIC KOKOBERA FEVER KRABBE DISEASE KUNJIN ENCEPHALITIS KUNJIN FEVER LACTOSE INTOLERANCE LATE INFANTILE BATTEN DISEASE LATE INFANTILE NEURONAL LIPOFUSCINOSIS LAZY LEUKOCYTE SYNDROME LCHAD DEFICIENCY LEAD POISONING LEBERS HEREDITARY OPTIC NEUROPATHY (LHON) LEGIONNAIRES DISEASE (LEGIONELLOSIS) LEIGHS SYNDROME LEISHMANIASIS LEPROSY LEPTOSPIROSIS LESCH-NYHAN SYNDROME LEUKAEMIA LEUKAEMIA ACUTE LYMPHOBLASTIC (ALL) LEUKAEMIA ACUTE MYELOBLASTIC (AML) LEUKAEMIA ACUTE PROMYELOCYTIC (APML) (FAB M3) LEUKAEMIA ADULT T- CELL LEUKAEMIA B CELL ACUTE LYMPHOBLASTIC LEUKAEMIA B CELL ACUTE LYMPHOCYTIC LEUKAEMIA CHRONIC GRANULOCYTIC (CGL) LEUKAEMIA CHRONIC LYMPHOCYTIC (CLL) LEUKAEMIA CHRONIC MYELOID (CML) LEUKAEMIA LYMPHATIC LEUKAEMIA, CHRONIC EOSINOPHILIC (CEL) LEUKAEMIA, EOSINOPHILIC (EL) LEUKAEMOID REACTIONS LEUKODYSPLASIA METACHROMATIC LEUKODYSTROPHY GLOBOID CELL LEUKODYSTROPHY METACHROMATIC LI FRAUMENI LIMB GIRDLE DYSTROPHY LIPIDOSES LIPODYSTROPHY PARTIAL LISSENCEPHALY LISTERIOSIS LIVER DISEASE LOAIASIS LONG CHAIN-3 HYDROXYACYL COA DEHYDROGENASE DEFICIENCY (LCHAD) LOWES SYNDROME LUNG DISEASE LUNG DISEASES - RESTRICTIVE LUPUS ERYTHEMATOSUS SYSTEMIC (SLE) LYME DISEASE LYMPHADENITIS LYMPHOCYTE ADHESION DEFICIENCY (LAD) LYMPHOCYTOSIS LYMPHOGRANULOMA VENEREUM LYMPHOMA LYMPHOMA NON-HODGKINS LYMPHOPROLIFERATIVE DISEASE LYMPHOPROLIFERATIVE DISEASES (B CELL) LYMPHOPROLIFERATIVE DISEASES (T CELL) LYMPHORETICULAR DISORDERS MAC-1 DEFICIENCY MACHADO JOSEPH DISEASE MACROAMYLASAEMIA MALABSORPTION MALAENA FETAL MALARIA MALIGNANT HYPERTHERMIA MANGANISM MAPLE SYRUP DISEASE MAPLE SYRUP URINE DISEASE MARFAN SYNDROME MAROTEAUX-LAMY SYNDROME MASTOCYTOSIS MCARDLE DISEASE MCARDLES DISEASE MCCARDLE DISEASE MEASLES MEDIUM CHAIN ACYL COA DEHYDROGENASE DEFICIENCY (MCAD) MELANESIAN OVALOCYSTOSIS MELANOMA MELANOMA HEREDITARY MELAS (MYOCLONIC EPILEPSY LACTIC ACIDOSIS AND STROKE) MELIOIDOSIS MENINGITIS MENINGITIS ASEPTIC MENINGITIS BACTERIAL MENINGITIS CARCINOMATOUS MENINGITIS CRYPTOCOCCAL MENINGITIS EOSINOPHILIC MENINGITIS MENINGOCOCCAL MENINGITIS VIRAL MENINGO - ENCEPHALITIS MENINGOCOCCAEMIA MENINGOCOCCAL DISEASE MENKES DISEASE MENOPAUSE, HIRSUTISM, VIRILISM MERRF (MYOCLONIC EPILEPSY WITH RAGGED RED FIBRES) METABOLIC SYNDROME METHAEMOGLOBIN REDUCTASE DEFICIENCY METHAEMOGLOBINAEMIA METHYLENE TETRAHYDROFOLATE REDUCTASE DEFICIENCY METHYLGLUTACONIC-3 ACIDURIA TYPE 2 METHYLMALONIC ACIDAEMIA / ACIDURIA MICROFIBILLAR DISORDERS MICROSCOPIC POLYARTERITIS MITOCHONDRIAL RESPIRATORY CHAIN DISORDERS MIXED CONNECTIVE TISSUE DISEASE MOLYBDENUM COFACTOR DEFECT MORQUIOS SYNDROME MOTOR NEURONE DISEASE MUCOLIPIDOSIS MUCOLIPIDOSIS TYPE I MUCOPOLYSACCHARIDOSES MUCOPOLYSACCHARIDOSES (I, II, IIIA, IIIB, IIIC, IIID, IVA, IVB, VI, VII) MUCOPOLYSACCHARIDOSES (MPS I, II, IIIA, IVA, VI) MUCOPOLYSACCHARIDOSIS TYPE IH OR IS MUCOPOLYSACCHARIDOSIS TYPE II MUCOPOLYSACCHARIDOSIS TYPE III B MUCOPOLYSACCHARIDOSIS TYPE IIIA MUCOPOLYSACCHARIDOSIS TYPE IIIC MUCOPOLYSACCHARIDOSIS TYPE IIID MUCOPOLYSACCHARIDOSIS TYPE IV MUCOPOLYSACCHARIDOSIS TYPE VI MUCOPOLYSACCHARIDOSIS TYPE VII MULTIPLE ACYLCoA DEHYDROGENASE DEFICIENCY MULTIPLE CARBOXYLASE DEFICIENCY MULTIPLE ENDOCRINE NEOPLASIA (MEN) MULTIPLE ENDOCRINE NEOPLASIA TYPE II (MEN II) MULTIPLE MYELOMA MULTIPLE SCLEROSIS MULTIPLE SULPHATASE DEFICIENCY MUMPS MUSCULAR ATROPHY NEUROGENIC MUSCULAR DYSTROPHY MUSCULAR DYSTROPHY DUCHENNE/BECKER MUSCULAR DYSTROPHY EMERY DREIFUSS MYALGIA MYASTHENIA GRAVIS MYCETOMA MYCOPLASMA INFECTION MYCOSES MYCOSIS FUNGOIDES MYELODYSPLASIA MYELOFIBROSIS IDIOPATHIC MYELOMA RENAL MYELOPROLIFERATIVE DISORDERS MYELOSUPPRESSION MYOCARDIAL INFARCTION (MI) MYOCARDITIS MYOCARDITIS UNKNOWN ORIGIN MYOCLONUS MYOPATHIES INHERITED AND ACQUIRED MYOPATHY MYOPATHY CONGENITAL MYOPATHY METABOLIC MYOPATHY MITOCHONDRIAL MYOPATHY NECROTIZING MYOPATHY X-LINKED MYOTUBULAR MYOPHOSPHORYLASE DEFICIENCY MYOSITIS MYOTONIA CONGENITA MYOTONIC DYSTROPHY N-ACETYLGALACTOSAMINIDASE DEFICIENCY NADH DIAPHORASE DEFICIENCY NARCOLEPSY NARP NEEDLESTICK INJURY NEMALINE MYOPATHY NEOPLASMS B CELL NEPHROLITHIASIS NEPHROTIC SYNDROME NEURAL TUBE DEFECT NEURAL TUBE DEFECTS NEUROBLASTOMA NEUROFIBROMATOSIS NEUROMUSCULAR DISEASES NEUROPATHOLOGICAL DISEASES NEUROPATHY NEUROPATHY ATAXIA RETINITIS PIGMENTOSA (NARP) NEUROPATHY PERIPHERAL NIEMANN-PICK DISEASE NIEMANN-PICK DISEASE TYPE A AND B NIEMANN-PICK DISEASE TYPE C NITROPRUSSIDE THERAPY MONITOR NOCARDIOSIS NOONANS SYNDROME NORRIE DISEASE OBESITY OBESITY/OVERWEIGHT OBSTRUCTIVE SLEEP APNOEA (OSA) OCKELBO VIRUS DISEASE OCULAR PHARYNGEAL MUSCULAR DYSTROPHY OCULOCUTANEOUS ALBINISM OLIGODENDROGLIOMA ONCHOCERCIASIS OPSOCLONUS - MYOCLONUS SYNDROME ORGANIC ACIDAEMIAS ORGANIC ACIDURIA ORGANOPHOSPHATE MONITORING ORGANOPHOSPHATE POISONING ORNITHINE TRANSCARBAMYLASE DEFICIENCY ORNITHINE TRANSCARBAMYLASE DEFICIENCY (OTC) OSTEOMALACIA OSTEOPOROSIS OVARIAN FAILURE PAGETS DISEASE PANCREATIC FISTULA PANCREATIC INSUFFICIENCY PANCREATITIS PANCREATITIS HEREDITARY PANCYTOPENIA PAPILLOMATA LARYNGEAL PARAGANGLIONOMA PARAINFLUENZA PARAPROTEIN NEUROPATHY PARAPROTEINAEMIA. PARATHYROID DISEASE PARKINSONS DISEASE PAROTITIS PAROXYSMAL COLD HAEMOGLOBINURIA (PCH) PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA (PNH) PEARSONS SYNDROME PELLAGRA PELVIC INFLAMMATORY DISEASE PEMPHIGUS VULGARIS PERIODIC FEVER PERIODIC PARALYSIS PERITONITIS PEROXISOMAL BIOGENESIS DISORDER PEROXISOMAL BIOGENESIS DISORDERS PERTUSSIS (WHOOPING COUGH) PEUTZ-JEGHERS SYNDROME PFEIFFER SYNDROME PHAEOCHROMOCYTOMA PHENYLKETONURIA (PKU) PHENYLKETONURIA (PKU) - PCR PHENYLKETONURIA (PKU) (PTS-6 DEFICIENCY) PHENYLKETONURIA (PKU) BIOPTERIN DEFECTIVE (PTS-6 DEFICIENCY) PHOSPHOFRUCTOKINASE DEFICIENCY PHOSPHOGLYCERATE KINASE (PGK) DEFICIENCY PHOSPHOLIPID SYNDROME PRIMARY PHOSPHOMANNOMUTASE DEFICIENCY PHOSPHORYLASE B KINASE DEFICIENCY PHOSPHORYLASE KINASE DEFICIENCY PINWORM DISEASE PITUITARY DISEASE PITUITARY HYPOFUNCTION PITYRIASIS VERSICOLOR PLACENTAL SULPHATASE DEFICIENCY PLATELET DISORDERS PRIMARY PLATELET FUNCTION DEFECTS PLEURAL EFFUSION PLEURAL EMPYEMA PNEUMOCOCCUS VACCINATION PNEUMONIA PNEUMONIA ATYPICAL PNEUMONIA LEGIONELLA PNEUMONIA MYCOPLASMA PNEUMONIA NEONATAL PNEUMONITIS HYPERSENSITIVITY POLIOMYELITIS POLYANGIITIS POLYARTERITIS POLYCYSTIC KIDNEY DISEASE POLYCYSTIC OVARY SYNDROME (PCO) POLYCYTHAEMIA POLYCYTHAEMIA RUBRA VERA (PRV) POLYDIPSIA PSYCHOGENIC POLYMYOSITIS POLYURIC SYNDROMES POMPES DISEASE (GLYCOGENOSIS TYPE II) PONTIAC FEVER PORPHYRIA PORPHYRIA - ACUTE INTERMITTENT PORPHYRIA (AIP) PORPHYRIA - ALA DEHYDRATASE DEFICIENCY (ALADD) PORPHYRIA - ALA DEHYDRATASE DEFICIENCY PORPHYRIA (ALADD) PORPHYRIA - CONGENITAL ERYTHROPOIETIC PORPHYRIA (CEP) PORPHYRIA - ERYTHROPOIETIC PROTOPORPHYRIA (EPP) PORPHYRIA - HEREDITARY COPROPORPHYRIA (HCP) PORPHYRIA - VARIEGATE PORPHYRIA (VP) PORPHYRIA ACUTE PORPHYRIA ACUTE INTERMITTENT (AIP) PORPHYRIA CUTANEA TARDA (PCT) - PCR PORPHYRIA CUTANEA TARDA HEREDITARY PORPHYRIA ERYTHROPOIETIC - PROTO PORPHYRIA HEREDITARY COPRO PORPHYRIA VARIEGATE POST TRANSFUSION PURPURA (PTP) PRADER WILLI SYNDROME PREGNANCY PREGNANCY EARLY ABNORMAL PREGNANCY ECTOPIC PRIMAPTERINURIA PRIMARY CARNITINE DEFICIENCY PRION DISEASES PROLACTINOMA PROPIONIC ACIDAEMIA PROPIONYL CoA CARBOXYLASE DEFICIENCY PROTEIN C DEFICIENCY PROTEIN LOSING ENTEROPATHIES PROTEIN LOSING ENTEROPATHY PROTEIN MALNUTRITION PROTEIN S DEFICIENCY PROTEINURIA PSEUDO B-GLUCURONIDASE DEFICIENCY PSEUDOARYL SULPHATASE A DEFICIENCY PSEUDOHYPOPARATHYROIDISM PSEUDOMEMBRANOUS COLITIS (PMC) PSITTACOSIS PUERPERAL FEVER PULMONARY EMBOLISM (PE) PULMONARY SURFACTANT PROTEIN B DEFICIENCY PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY PURTILLOS SYNDROME PYELONEPHRITIS PYRIMIDINE-5-NUCLEOTIDASE DEFICIENCY PYRUVATE CARBOXYLASE DEFICIENCY PYRUVATE DEHYDROGENASE DEFICIENCY PYRUVATE KINASE DEFICIENCY Q FEVER RABIES REFSUM DISEASE REFSUM DISEASE INFANTILE RENAL ARTERY STENOSIS RENAL DIALYSIS RENAL DISEASE RENAL DISEASE TUBULAR RENAL FAILURE RENAL FAILURE CHRONIC RENAL MYELOMA RENAL TUBULAR DISEASE RETINAL OCCLUSION RETINOBLASTOMA RETT SYNDROME REYES SYNDROME Rh DISEASE RHABDOMYOLYSIS RHABDOMYOSARCOMA ALVEOLAR RHIZOMELIC CHONDRODYSPLASIA PUNCTATA (RCDP) RHIZOMELIC CHONDROPLASIA PUNCTATA TYPE 1 RHIZOMELIC CHONDROPLASIA PUNCTATA TYPE 2 RINGWORM RIVER BLINDNESS ROSEOLA INFANTUM ROSS RIVER FEVER ROTOR SYNDROME RUBELLA RUSSELL SILVER SYNDROME SAETHRE-CHOTZEN SYNDROM SALLA DISEASE SALMONELLA TYPHI SALMONELLOSIS SANDHOFF DISEASE SANFILIPPO SYNDROME SANFILIPPO SYNDROME C SANFILIPPO SYNDROME D SANTAVUORI DISEASE SARCOIDOSIS SCABIES SCHEIE DISEASE SCHINDLER DISEASE SCHISTOSOMIASIS SCHWACHMAN SYNDROME SCHWACHMAN-DIAMOND SCLERODERMA SCLEROSIS SYSTEMIC SCURVY SEPSIS SEPTICAEMIA MENINGOCOCCAL SEROTONIN DEFICIENCY SEROTONIN DEFICIENCY DISEASES SEVERE COMBINED IMMUNODEFICENCY SYNDROME - X-LINKED SEVERE COMBINED IMMUNODEFICIENCY SYNDROME (SCIDS) SEZARY SYNDROME SFTPB RELATED PULMONARY ALVEOLAR PROTEINOSIS SHIGELLOSIS SHINGLES (HERPES ZOSTER) SHORT CHAIN ACYL CoA DEHYDROGENASE DEFICIENCY SIADH (SYNDROME OF INAPPROPRIATE SECRETION OF ADH) SIALIC ACID STORAGE DISEASE INFANTILE FREE SIALIDOSIS SIALURIA SICKLE BETA THALASSAEMIA SICKLE CELL DISEASE SIXTH DISEASE SJOGRENS SYNDROME SLEEPING SICKNESS SLY SYNDROME SMITH-LEMLI-OPITZ SYNDROME SMOKING CIGARETTES South East Asian Ovalocytosis SPEILMEYER-VOGT DISEASE SPINAL MUSCULAR ATROPHY SPINOCEREBELLAR ATAXIA (SCA) SPOTTED FEVER AUSTRALIAN SPOTTED FEVER FLINDERS ISLAND SPOTTED FEVER MEDITERRANEAN SPOTTED FEVER ROCKY MOUNTAIN STEATHORRHOEA STEM CELL TRANSPLANT STEROID SULPHATASE DEFICIENCY STRONGYLOIDIASIS SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY SULPHITE OXIDASE DEFICIENCY SUXAMETHONIUM SENSITIVITY SYPHILIS SYSTEMIC LUPUS ERYTHEMATOSUS (SLE) SYSTEMIC LUPUS ERYTHEMATOSUS (SLE) DRUG INDUCED SYSTEMIC LUPUS ERYTHEMATOSUS (SLE) SUBACUTE TAY SACHS DISEASE TAY SACHS DISEASE (GM2 GANGLIOSIDOSIS VAR B) TESTICULAR FEMINIZATION TETANUS VACCINATION THALASSAEMIA THALASSAEMIA ALPHA THALASSAEMIA BETA THALASSAEMIA DELTA THALASSAEMIA DELTA BETA THALASSAEMIA HPFH (HEREDITARY PERSISTENCE OF FETAL HAEMOGLOBIN) THOMSONS DISEASE THROMBOCYTHAEMIA ESSENTIAL THROMBOCYTOPAENIA TYPE II HEPARIN INDUCED THROMBOCYTOPAENIC PURPURA IDIOPATHIC (ITP) THROMBOCYTOPAENIC PURPURA IMMUNE (ITP) THROMBOCYTOPAENIC PURPURA THROMBOTIC (TTP) THROMBOPHILIA THROMBOPHILIA HEREDITARY RECURRENT THROMBOSIS THRUSH THYMOMA THYROID DISEASE TICK TYPHUS MEDITERRANEAN TICK TYPHUS QUEENSLAND TINEA TINEA VERSICOLOR TOMACULOUS NEUROPATHY TOTAL SULPHATASE DEFICIENCY TOXOCARIASIS TOXOPLASMOSIS TRANSFUSION REACTION TRANSPLANT MONITORING TRAPS (TUMOUR NECROSIS FACTOR RECEPTOR ASSOCIATED PERIODIC SYNDROME) TRICHINOSIS TRIHYDROXYCHOLESTANOIC ACIDAEMIA TRIMETHYLAMINURIA TRIOSEPHOSPHATE ISOMERASE (TPI) DEFICIENCY TROPICAL PARAPARESIS TRYPANOSOMIASIS AFRICAN TRYPANOSOMIASIS AMERICAN TUBERCULOSIS TUBEROUS SCLEROSIS TUBULAR PROTEINURIA TUMOUR ENDOCRINE TYPHOID TYPHUS TYPHUS EPIDEMIC TYPHUS MURINE TYPHUS SCRUB TYROSINAEMIA TYROSINAEMIA TYPE I ULCER ULCERATIVE COLITIS URETHRITIS URINARY TRACT INFECTION VALLEY FEVER VARICELLA (CHICKEN POX) VASCULITIS VASCULITIS SYSTEMIC VENTILATION / PERFUSION (V/Q) ABNORMALITY VIRILISM VISCERAL LARVA MIGRANS VITAMIN A DEFICIENCY (NIGHT BLINDNESS) VITAMIN B1 (THIAMINE) DEFICIENCY VITAMIN B12 (COBALAMIN) DEFICIENCY VITAMIN B2 (RIBOFLAVIN) DEFICIENCY VITAMIN B3 (NIACIN) DEFICIENCY VITAMIN B6 (PYRIDOXINE) DEFICIENCY VITAMIN C DEFICIENCY VITAMIN D 1,25 HYDROXY DEFICIENCY VITAMIN D 25 HYDROXY DEFICIENCY VITAMIN E DEFICIENCY VITAMIN K DEFICIENCY VON GIERKES DISEASE VON HIPPEL LINDAU DISEASE VON WILLEBRAND DISEASE TYPE 2N VON WILLEBRANDS DISEASE WAGR SYNDROME WALDENSTROMS MACROGLOBULINAEMIA WARFARIN THERAPY MONITOR WEGENERS GRANULOMATOSIS WEILS DISEASE WERNICKE - KORSAKOFF SYNDROME WEST NILE FEVER WHIPPLES DISEASE WILMS TUMOUR WILSONS DISEASE WISKOTT-ALDRICH SYNDROME WOLMAN DISEASE X - ALD XLINKED AGAMMAGLOBULINAEMIA X-LINKED DISORDERS X-LINKED HYDROCEPHALUS X-LINKED HYPER IgM SYNDROME XLINKED LYMPHOPROLIFERATIVE DISEASE (DUNCANS) X-LINKED LYMPHOPROLIFERATIVE SYNDROME X-LINKED MENTAL RETARDATION (XLMR) X-SCID Y CHROMOSOME MICRODELETIONS YELLOW FEVER YERSINIOSIS ZELLWEGER SYNDROME ZOLLINGER ELLINSON SYNDROME (ZE)
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