- 1101. congenital hypertension
- [persistently high arterial blood pressure occurring in or affecting more members of a family than would be expected by chance. ( CSP )] (UMLS (CSP) C0598428) =Disease or Syndrome ;
=Blood Pressure, High;
| - 1151. Congenital Spondylolysis
- (UMLS (NCI) C0840926) =Congenital Abnormality
|
- 1102. congenital hypoplastic anemia
- [An inborn condition characterized by deficiencies of red cell precursors that sometimes also includes LEUKOPENIA and THROMBOCYTOPENIA. ( MSH )] (UMLS (CSP) C0949116) =Congenital Abnormality; Disease or Syndrome
| - 1152. Congenital Spondylolysis, Lumbosacral Region
- (UMLS (NCI) C0432162) =Congenital Abnormality ;
|
- 1103. Congenital hypothyroidism
- [condition due to congenital lack of thyroid hormone, marked by arrested physical and mental development, dystrophy of the bones and soft parts, and lowered basal metabolism; it is the congenital form of thyroid deficiency, while myxedema is the acquired form. ( CSP )] (UMLS (ICD9CM) C0010308) =Congenital Abnormality; Disease or Syndrome =Bone Diseases, Endocrine;
dwarfism;
hypothyroidism;
congenital disorder | - 1153. congenital sucrose isomaltose malabsorption
- [characterized by the deficiency or absence of the enzymes sucrase and isomaltase existing at, and usually before birth; this enzyme complex (sucrase-isomaltase) assists in the breakdown of a certain sugar (ie, sucrose) and certain products of starch digestion (dextrins); only evident soon after birth when sucrose or starches, such as found in modified milk formulas with sucrose or polycose, are ingested by an affected infant, breast-fed infants or those on lactose-only formula manifest no symptoms until such time as sucrose (found in fruit juices, solid foods, and/or some medications) is introduced into the diet. ( CSP )] (UMLS (CSP) C1283620) sucrase alpha dextrinase deficiency;
sucrase isomaltase deficiency =Disease or Syndrome =Carbohydrate Metabolism, Inborn Errors;
enzyme deficiency;
inborn biological transport disorder;
|
- 1104. Congenital Hypothyroidism with Ectopic Thyroid
- (UMLS (NCI) C0342155) =Congenital Abnormality ;
| - 1154. Congenital syphilis
- [Syphilis acquired in utero and manifested by any of several characteristic tooth (Hutchinson's teeth) or bone malformations and by active mucocutaneous syphilis at birth or shortly thereafter. Ocular and neurologic changes may also occur. ( MSH )] (UMLS (ICD9CM) C0039131) =Disease or Syndrome =Infant, Newborn, Diseases;
syphilis |
- 1105. congenital ichthyosis
- [skin disorders characterized by dryness, roughness, and scaliness, due to hypertrophy of the stratum corneum epidermis that exist at, and usually before, birth regardless of their causation; most ichthyoses are genetically determined. ( CSP )] (UMLS (CSP) C0020758) =Congenital Abnormality; Disease or Syndrome ;
=Genetic Condition;
Congenital anomalies of the integument | - 1155. Congenital T-Cell Immunodeficiency
- (UMLS (NCI) C1333147) =Disease or Syndrome ;
|
- 1106. congenital immunodeficiency
- [ ] (UMLS (CSP) C0853602) =Congenital Abnormality; Disease or Syndrome
| - 1156. Congenital Thyroid Aplasia
- (UMLS (NCI) C0342152) =Congenital Abnormality; Disease or Syndrome
|
- 1107. CONGENITAL INFEC NEC
- [ ] (UMLS (ICD9CM) C0158946) =Disease or Syndrome
| - 1157. Congenital Thyroid Disorder
- (UMLS (NCI) C0852066) Congenital Thyroid Gland Disorder =Congenital Abnormality; Disease or Syndrome
|
- 1108. congenital infection
- [infections acquired in utero and persisting after birth; this term applies maninly to the infant, in contrast to PREGNANCY INFECTION, which applies mainly to the mother and fetus. ( CSP )] (UMLS (CSP) C0275544) =Disease or Syndrome =infection;
congenital disorder | - 1158. Congenital Thyroid Gland Hypoplasia
- (UMLS (NCI) C0342153) =Congenital Abnormality; Disease or Syndrome
|
- 1109. Congenital Infundibular Stenosis
- [Narrowing below the PULMONARY VALVE or well below it in the infundibuluar chamber where the pulmonary artery originates, usually caused by a defective VENTRICULAR SEPTUM or presence of fibrous tissues. It is characterized by restricted blood outflow from the RIGHT VENTRICLE into the PULMONARY ARTERY, exertional fatigue, DYSPNEA, and chest discomfort. ( MSH )] (UMLS (NCI) C0034084) =Disease or Syndrome =pulmonary valve stenosis;
| - 1159. Congenital Toxoplasmosis
- [Passed from mother to fetus. ( NCI )] (UMLS (NCI) C0040560) =Disease or Syndrome ;
=Infant, Newborn, Diseases;
TOKSOPLASMOOSI;
Central Nervous System Protozoal Infections;
|
- 1110. Congenital Iodine Deficiency Hypothyroidism
- (UMLS (NCI) C0342200) =Congenital Abnormality; Disease or Syndrome
| - 1160. CONGENITAL URETEROCELE
- [ ] (UMLS (ICD9CM) C0474873) =Congenital Abnormality
|
- 1111. congenital kidney disorder
- [impairments of health or a condition of abnormal functioning of the kidney that exist at, and usually before, birth regardless of their causation. ( CSP )] (UMLS (CSP) C0543793) =Disease or Syndrome =Kidney Disease;
congenital disorder =polycystic kidney;
cerebrohepatorenal syndrome | - 1161. congenital vision disorder
- [visual impairments limiting one or more of the basic functions of the eye: visual acuity, dark adaptation, color vision, or peripheral vision existing at, and usually before, birth regardless of causation. ( CSP )] (UMLS (CSP) C0596373) =Disease or Syndrome ;
=Congenital anomalies of eye;
vision disorder |
- 1112. Congenital Kyphosis
- (UMLS (NCI) C0265673) =Congenital Abnormality ;
| - 1162. Congenital, Familial and Genetic Disorder Class
- [A class of disorders that encompasses conditions resulting from a congenital, familial hereditary trait or genetic abnormality as is manifested by a characterstic set of symptoms and signs. (NCI) ( NCI )] (UMLS (NCI) C0851352) CONGENITAL, FAMILIAL AND GENETIC DISORDERS;
=Congenital Abnormality |
- 1113. congenital laryngismus
- [ ] (UMLS (CSP) C0598229) =Congenital Abnormality; Disease or Syndrome
| - 1163. Congestion or hemorrhage of prostate
- [ ] (UMLS (ICD9CM) C0156295) =Pathologic Function ;
|
- 1114. Congenital Lens Disorder
- (UMLS (NCI) C0339350) =Congenital Abnormality
| - 1164. Congestive
- [Relating to or affected by an abnormal collection of blood or other fluid. ( NCI )] (UMLS (NCI) C0742742) =Qualitative Concept ;
|
- 1115. Congenital Leucocyte Abnormality
- (UMLS (NCI) C0017377) =Disease or Syndrome
| - 1165. congestive atelectasis
- [ ] (UMLS (CSP) C0205938) =Disease or Syndrome ;
|
- 1116. Congenital Macrocephaly
- (UMLS (NCI) C0877524) Congenital Megacephaly;
Congenital Megalocephaly;
=Congenital Abnormality | - 1166. CONGN ANOML ABD WALL NEC
- [ ] (UMLS (ICD9CM) C0490010) =Congenital Abnormality
|
- 1117. Congenital Macular Corneal Dystrophy
- (UMLS (NCI) C0521561) =Congenital Abnormality
| - 1167. Congo hemorrhagic fever virus
- [tick borne nairovirus, causes often fatal hemorrhagic fever in humans. ( CSP )] (UMLS (CSP) C0009743) =Virus ;
=Bunyaviridae;
|
- 1118. Congenital Melanocytic Nevus
- (UMLS (NCI) C1318558) Congenital Melanocytic Nevus of Skin;
Congenital Melanocytic Nevus of the Skin;
Congenital Nevus of Skin;
Congenital Nevus of the Skin;
Congenital Pigmented Nevus of Skin;
Congenital Pigmented Nevus of the Skin;
Congenital Pigmented Skin Nevus;
Congenital Skin Nevus =Neoplastic Process ;
| - 1168. Congo red stain
- [Stain, Congo red ( HL7V3.0 )] (UMLS (HL7) C1293958) =Laboratory Procedure =ObservationMethod;
|
- 1119. Congenital Metabolic Disorder
- [errors in metabolic processes resulting from inborn genetic mutations that are inherited or acquired in utero. ( CSP )] (UMLS (NCI) C0025521) =Disease or Syndrome =Genetic Condition;
Metabolic Disease =Adrenal Hyperplasia, Congenital;
Amino Acid Metabolism, Inborn Errors;
Carbohydrate Metabolism, Inborn Errors;
G6PD deficiency;
hereditary hyperbilirubinemia;
hypophosphatasia;
inborn metal metabolism disorder;
Albright's hereditary osteodystrophy;
purine/pyrimidine metabolism disorder;
inborn lysosomal enzyme disorder;
inborn lipid/lipoprotein disorder;
alpha 1 antitrypsin deficiency;
pyruvate kinase deficiency;
inborn immunodeficiency;
inborn biological transport disorder;
PGK deficiency;
amyloid disease;
Carbohydrate Metabolism, Inborn Errors;
Glucosephosphate Dehydrogenase Deficiency;
hereditary hyperbilirubinemia;
Dubin Johnson syndrome;
Lipid Metabolism, Inborn Errors;
inborn metal metabolism disorder;
DIS PORPHYRIN METABOLISM;
Hutchinson Gilford syndrome;
purine/pyrimidine metabolism disorder;
inborn renal tubular transport disorder;
inborn lysosomal enzyme disorder;
Brain Diseases, Metabolic, Inborn;
| - 1169. Congo-Crimean Hemorrhagic Fever
- [A severe, often fatal disease in humans caused by the Crimean-Congo hemorrhagic fever virus (HEMORRHAGIC FEVER VIRUS, CRIMEAN-CONGO). ( MSH )] (UMLS (NCI) C0019099) =Disease or Syndrome ;
=Bunyaviridae Infections;
hemorrhagic fever;
Tick-Borne Diseases;
|
- 1120. CONGENITAL MONOPLEGIA
- [ ] (UMLS (ICD9CM) C0154698) =Disease or Syndrome
| - 1170. Congregational
- (UMLS (HL7) C0682432) =Population Group =Religious Affiliation;
|
- 1121. congenital muscle disorder
- [impairments of health or a condition of abnormal functioning of muscles that exist at, and usually before, birth regardless of their causation. ( CSP )] (UMLS (CSP) C1655035) =Disease or Syndrome ;
=muscle disorder;
congenital disorder =congenital neuromuscular disorder | - 1171. Congress
- [The U.S. legislature, consisting of the Senate and the House of Representatives. ( NCI )] (UMLS (NCI) C0009753) =Organization ;
|
- 1122. Congenital Muscular Torticollis
- [A congenital benign neoplasm arising from the sternocleidomastoid muscle in infants. It is characterized by the presence of plump spindle cells, and collagenous stroma formation. ( NCI )] (UMLS (NCI) C0549175) =Disease or Syndrome
| - 1172. conie
- [Single genus in the family Ochotonidae. ( MSH )] (UMLS (CSP) C0324891) =Mammal
|
- 1123. Congenital musculoskeletal anomalies
- [Congenital structural abnormalities and deformities of the musculoskeletal system.(MSH)] (UMLS (ICPC) C0151491) (Congenital musculoskeletal anomalies; SORTZETIKO ANOMALIA; Medfodt misdannelse; Aangeboren afw bewegingsapparaat; SYNNYNNAISET EPAMUODOSTUMAT; Anomalies confenitales; angeborene Missbild Bewegungsapparat; (108); veleszuletett rendellenesseg; Anomalie congenite; MEDFODTE FEIL; Malformacoes congenitas; Anomalias congenitas; MEDFODDA MISSBILDNINGAR) =Congenital Abnormality; Disease or Syndrome =Aangeboren afwijking spijsvert org; Musculoskeletal Diseases; musculoskeletal; Diagnosis/Diseases Component =Arthrogryposis; Funnel Chest; Congenital dislocation of hip; Klippel-Feil syndrome; Synostosis; CONGEN LIMB ANOMALY NOS; Gastroschisis; Craniofacial Abnormalities
| - 1173. Conifera
- [plant division of gymnosperms including cone-bearing trees and shrubs, and yews. ( CSP )] (UMLS (CSP) C0330199) =Plant =gymnosperm;
|
- 1124. Congenital musculoskeletal deformities of sternocleidomastoid muscle
- (UMLS (ICD9CM) C0345380) =Congenital Abnormality ;
| - 1174. CONJOINED TWINS
- (UMLS (ICD9CM) C0041428) =Congenital Abnormality =Monsters;
|
- 1125. Congenital Nephrotic Syndrome
- (UMLS (NCI) C0268713) =Disease or Syndrome
| - 1175. Conjugate
- [A compound formed by the union of two entities or compounds. ( NCI )] (UMLS (NCI) C0301869) =Immunologic Factor; Indicator, Reagent, or Diagnostic Aid
|
- 1126. Congenital neurologic anomalies
- [structural or functional abnormalities of the central or peripheral nervous system existing at birth and often before birth, resulting primarily from defects of embryogenesis.(CSP)] (UMLS (ICPC) C0497552) (Congenital neurologic anomalies; (194); (115); (116); (104); (105); (106); (108); (119); (133); (130); (122); (123)) Congenital neurologic anomalies =Congenital Abnormality; Disease or Syndrome =Aangeboren afwijking spijsvert org; CNS DISORDER NOS; congenital disorder; =Dysautonomia, Familial; congenital neuromuscular disorder; Intracranial Arteriovenous Malformations; Dandy-Walker Syndrome; Hydranencephaly; neural tube defect; Hereditary Motor and Sensory Neuropathies; Hereditary Sensory and Autonomic Neuropathies; holoprosencephaly; Central Nervous System Cyst; Central Nervous System Vascular Malformation
| - 1176. Conjugate Vaccine
- [Semisynthetic vaccines consisting of polysaccharide antigens from microorganisms attached to protein carrier molecules. The carrier protein is recognized by macrophages and T-cells thus enhancing immunity. Conjugate vaccines induce antibody formation in people not responsive to polysaccharide alone, induce higher levels of antibody, and show a booster response on repeated injection. ( MSH )] (UMLS (NCI) C0206515) =Pharmacologic Substance; Immunologic Factor ;
|
- 1127. congenital neuromuscular disorder
- [diseases existing at birth and often before birth, which effect the motor neuron, peripheral nervous system and certain muscular diseases; manifestations include muscle weakness, fasciculation, atrophy, spasm, myokymia, hypertonic, hypotonia and myalgias. ( CSP )] (UMLS (CSP) C0596371) =Congenital Abnormality; Disease or Syndrome =congenital nervous system disorder;
congenital muscle disorder =amyotonia congenita;
myotonia atrophica;
myotonia congenita;
| - 1177. Conjugated Estrogens
- [Purified orally bioavailable female sex hormones isolated from pregnant mare urine or synthetically derived from plant materials and primarily conjugated as sulfate esters. Estrogen binds to and activates specific nuclear receptors, which, in turn, bind to estrogen response elements (EREs) in target genes, resulting in histone acetylation, alteration of chromatin conformation, and initiation of transcription. (NCI04) ( NCI )] (UMLS (NCI) C0014938) =Steroid; Pharmacologic Substance; Hormone =[HS300] ESTROGENS;
[GU500] ESTROGENS, VAGINAL;
Unclassified Ingredients;
=Estrogens, Conjugated (USP) 0.45 MG;
Estrogens, Conjugated (USP) 0.5 MG/ML;
Estrogens, Conjugated (USP) 2 MG;
Estrogens, Conjugated (USP) 2 MG/ML;
Estrogens, Conjugated (USP) 200000 UNT/ML;
Estrogens, Conjugated (USP) 0.3 MG;
Estrogens, Conjugated (USP) 1.25 MG;
Estrogens, Conjugated (USP) 5 MG/ML;
Estrogens, Conjugated (USP) 0.625 MG;
Estrogens, Conjugated (USP) 0.9 MG;
Estrogens, Conjugated (USP) 2.5 MG;
ESTROGENS,CONJUGATED 025 MG;
ESTROGENS,CONJUGATED 28TAB X 0.625 MG;
ESTROGENS,CONJUGATED DAY1-28 X 0.625 MG;
ESTROGENS,CONJUGATED 0.625 MG/GM;
|
- 1128. Congenital Neuropathy
- (UMLS (NCI) C0920187) =Congenital Abnormality
| - 1178. conjugated polyene
- [ ] (UMLS (CSP) C0598131) =Organic Chemical
|
- 1129. CONGENITAL NEUTROPENIA
- [ ] (UMLS (ICD9CM) C0340970) =Disease or Syndrome
| - 1179. CONJUN CUL-DE-SAC RX NEC
- [ ] (UMLS (ICD9CM) C0176200) =Therapeutic or Preventive Procedure
|
- 1130. Congenital Nevus Araneus
- (UMLS (NCI) C0542118) =Congenital Abnormality ;
| - 1180. CONJUNC FREE GRAFT NEC
- [ ] (UMLS (ICD9CM) C0176201) =Therapeutic or Preventive Procedure
|
- 1131. congenital nonhemolytic jaundice
- [A benign familial disorder, transmitted as an autosomal dominant trait. It is characterized by low-grade chronic hyperbilirubinemia with considerable daily fluctuations of the bilirubin level. ( MSH )] (UMLS (CSP) C0017551) =Disease or Syndrome ;
=hereditary hyperbilirubinemia;
| - 1181. CONJUNC/LID ADHESIOLYSIS
- [ ] (UMLS (ICD9CM) C0176203) =Therapeutic or Preventive Procedure
|
- 1132. Congenital nuclear cataract
- [ ] (UMLS (ICD9CM) C0158551) =Congenital Abnormality; Disease or Syndrome
| - 1182. conjunctiva
- [mucous membrane that lines the inner surface of the eyelids and the anterior part of the sclera. ( CSP )] (UMLS (CSP) C0009758) =Body Part, Organ, or Organ Component ;
=EYE;
Body Part |
- 1133. CONGENITAL NYSTAGMUS
- [Nystagmus present at birth or caused by lesions sustained in utero or at the time of birth. It is usually pendular, and is associated with ALBINISM and conditions characterized by early loss of central vision. Inheritance patterns may be X-linked, autosomal dominant, or recessive. (Adams et al., Principles of Neurology, 6th ed, p275) ( MSH )] (UMLS (ICD9CM) C0700501) =Congenital Abnormality; Disease or Syndrome ;
=Infant, Newborn, Diseases;
nystagmus | - 1183. Conjunctiva
- (UMLS (HL7) C1546576) =Intellectual Product =Specimen Source Codes;
|
- 1134. Congenital or acquired abnormality of vagina complicating pregnancy, childbirth, or the puerperium
- [ ] (UMLS (ICD9CM) C0157045) =Disease or Syndrome; Anatomical Abnormality
| - 1184. Conjunctiva
- (UMLS (HL7) C1550624) =Body Substance =SpecimenEntityType;
|
- 1135. Congenital or acquired abnormality of vulva complicating pregnancy, childbirth, or the puerperium
- [ ] (UMLS (ICD9CM) C0157051) =Disease or Syndrome; Anatomical Abnormality
| - 1185. Conjunctiva Cyst
- [Abnormal fluid filled sac within the conjunctiva. ( NCI )] (UMLS (NCI) C0155170) =Finding ;
|
- 1136. congenital oral defect
- [ ] (UMLS (CSP) C0920446) =Congenital Abnormality
| - 1186. CONJUNCTIVA DISORDER NEC
- [ ] (UMLS (ICD9CM) C0155171) =Disease or Syndrome ;
|
- 1137. congenital oral/facial/cranial defect
- [structural deformities, malformations, or other abnormalities of the cranium, oral and facial bones, muscles, cartilage, etc, that exist at, and usually before, birth regardless of their causation. ( CSP )] (UMLS (CSP) C0596372) =Congenital Abnormality ;
=congenital disorder;
=cleft lip;
cleft palate;
craniofacial dysostosis;
Craniosynostoses;
congenital palatopharyngeal defect;
Smith Magenis syndrome | - 1187. CONJUNCTIVA DISORDER NOS
- (UMLS (ICD9CM) C0009759) =Disease or Syndrome ;
=Disorder of eye, unspecified;
=Conjunctiva Neoplasm;
conjunctivitis;
Pterygium;
CONJUNCTIVAL XEROSIS;
|
- 1138. Congenital osteodystrophies
- [ ] (UMLS (ICD9CM) C0375536) =Congenital Abnormality
| - 1188. CONJUNCTIVA DX PROC NEC
- [ ] (UMLS (ICD9CM) C0176195) =Diagnostic Procedure
|
- 1139. Congenital other anomalies of lung
- [ ] (UMLS (ICD9CM) C0478018) =Congenital Abnormality
| - 1189. Conjunctiva Epidermoid Carcinoma
- (UMLS (NCI) C0346359) =Neoplastic Process
|
- 1140. congenital palatopharyngeal defect
- [abnormalities in which the soft palate fails to reach the posterior pharyngeal wall, existing at, and usually before, birth regardless of their causation. ( CSP )] (UMLS (CSP) C0178567) =Congenital Abnormality ;
=congenital oral/facial/cranial defect;
| - 1190. CONJUNCTIVA INCISION NEC
- [ ] (UMLS (ICD9CM) C0176193) =Therapeutic or Preventive Procedure
|
- 1141. CONGENITAL PES PLANUS
- [ ] (UMLS (ICD9CM) C0392477) =Congenital Abnormality
| - 1191. Conjunctiva Intraepithelial Neoplasia
- (UMLS (NCI) C1333148) Conjunctival Intraepithelial Neoplasia;
Intraepithelial Neoplasia of Conjunctiva;
Intraepithelial Neoplasia of the Conjunctiva =Neoplastic Process ;
|
- 1142. Congenital Phimosis
- (UMLS (NCI) C0345326) =Congenital Abnormality ;
| - 1192. Conjunctiva Melanoma
- [A malignant melanoma within the conjunctiva of the eye. ( NCI )] (UMLS (NCI) C0346360) =Neoplastic Process
|
- 1143. CONGENITAL PNEUMONIA
- [ ] (UMLS (ICD9CM) C0158935) =Disease or Syndrome
| - 1193. Conjunctiva Neoplasm
- [Tumors or cancer of the CONJUNCTIVA. ( MSH )] (UMLS (NCI) C0009761) =Neoplastic Process =CONJUNCTIVA DISORDER NOS;
eye neoplasm |
- 1144. CONGENITAL QUADRIPLEGIA
- [ ] (UMLS (ICD9CM) C0154697) =Congenital Abnormality; Disease or Syndrome
| - 1194. CONJUNCTIVA PIGMENTATION
- [ ] (UMLS (ICD9CM) C0155163) =Disease or Syndrome ;
|
- 1145. Congenital reduction deformities of brain
- (UMLS (ICD9CM) C0079157) =Congenital Abnormality ;
| - 1195. CONJUNCTIVA VASC ANOMALY
- (UMLS (ICD9CM) C0042370) =Disease or Syndrome; Anatomical Abnormality ;
|
- 1146. CONGENITAL RENAL CYST
- [ ] (UMLS (ICD9CM) C0268800) =Congenital Abnormality
| - 1196. CONJUNCTIVAL CONCRETIONS
- [ ] (UMLS (ICD9CM) C0155162) =Acquired Abnormality; Disease or Syndrome
|
- 1147. congenital reproductive system disorder
- [reproductive system disorders that are present at birth regardless of their causation. ( CSP )] (UMLS (CSP) C0553529) =Congenital Abnormality; Disease or Syndrome =Genital Disorders;
congenital disorder =Cryptorch/niet ingedaalde testis;
hermaphroditism;
pseudohermaphroditism;
testicular feminization;
| - 1197. CONJUNCTIVAL DEGEN NOS
- [ ] (UMLS (ICD9CM) C0155160) =Disease or Syndrome
|
- 1148. congenital respiratory disorder
- [structural abnormalities of the respiratory system that exist at, and usually before, birth regardless of their causation. ( CSP )] (UMLS (CSP) C0702198) =Disease or Syndrome ;
=DISEASES OF THE RESPIRATORY SYSTEM;
congenital disorder =idiopathic respiratory distress of newborn | - 1198. Conjunctival degenerations and deposits
- [ ] (UMLS (ICD9CM) C0155159) =Acquired Abnormality
|
- 1149. CONGENITAL RUBELLA
- [Transplacental infection of the fetus with rubella usually in the first trimester of pregnancy, as a consequence of maternal infection, resulting in various developmental abnormalities in the newborn infant. They include cardiac and ocular lesions, deafness, microcephaly, mental retardation, and generalized growth retardation. (From Dorland, 27th ed) ( MSH )] (UMLS (ICD9CM) C0035921) =Disease or Syndrome =Abnormalities, Multiple;
ademet | - 1199. CONJUNCTIVAL DEPOSITS
- [ ] (UMLS (ICD9CM) C0162280) =Acquired Abnormality; Disease or Syndrome
|
- 1150. congenital skeletal disorder
- [structural abnormalities and deformities of the skeletal system that exist at, and usually before, birth regardless of their causation. ( CSP )] (UMLS (CSP) C0178568) =Congenital Abnormality ;
=congenital disorder;
skeletal disorder =achondroplasia;
Cartilage Development Disorder;
Marfan syndrome;
brittle bone disease;
osteosclerosis;
spina bifida;
Holt Oram syndrome;
fusion failure | - 1200. CONJUNCTIVAL DIPHTHERIA
- (UMLS (ICD9CM) C0012554) =Disease or Syndrome
|
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