V18.2 is a legacy non-billable code used to specify a medical diagnosis of family history of anemia. This code was replaced on September 30, 2015 by its ICD-10 equivalent. ICD-9:
2007 ICD-9-CM Diagnosis Code V18.2 Family history of anemia Short description: FAMILY HX-ANEMIA. ICD-9-CM V18.2 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, V18.2 should only be used for claims with a date of service on or before September 30, 2015.
ICD-9 Code V18.2 -Family history of anemia- Codify by AAPC Family history of anemia (V18.2) ICD-9 code V18.2 for Family history of anemia is a medical classification as listed by WHO under the range -PERSONS WITH POTENTIAL HEALTH HAZARDS RELATED TO PERSONAL AND FAMILY HISTORY (V10-V19). Subscribe to Codify and get the code details in a flash.
Apr 30, 2022 · V18.2 Family history of anemia ICD-9-CM Vol. 1 Diagnostic Codes V18.2 - Family history of anemia The above description is abbreviated. This code description may also have Includes, Excludes, Notes, Guidelines, Examples and other information. Access to this feature is available in the following products: Find-A-Code Essentials HCC Plus
195.2 Abdominal cavity#N#173.5 Abdominal wall (skin)#N#154.3 Anus (anal)#N#156.9 Biliary tract (cholangiocarcinoma), unspecified site#N#188.9 Bladder, unspecified site#N#233.7 Bladder, in situ#N#191.9 Brain, unspecified site#N#174.9 Breast, female, unspecified site#N#233.0 Breast, in situ (DCIS)#N#175.9 Breast, male, unspecified site#N#162.9 Bronchus, unspecified site#N#180.9 Cervix (cervival), unspecified site#N#233.1 Cervix uteri, in situ#N#170.9 Chondrosarcoma#N#153.9 Colon (colorectal), unspecified site#N#182.0 Endometrium (endometrial)#N#150.9 Esophagus (esophageal), unspecified site#N#170.9 Ewing's sarcoma#N#159.9 Gastrointestinal tract, unspecified site#N#184.9 Genital, female, unspecified site#N#187.9 Genital, male, unspecified site#N#153.9 Intestine (bowel), large, unspecified site#N#152.9 Intestine (bowel), small, unspecified site#N#176.9 Kaposi's Sarcoma, unspecified site#N#189.0 Kidney (renal)#N#155.0 Liver (hepatocellular), primary#N#155.2 Liver, not specified as primary or secondary#N#162.9 Lung (adenocarcinoma/squamous cell carcinoma), unspecified site#N#209.36 Merkel cell carcinoma#N#145.9 Mouth, unspecified site#N#147.9 Nasopharynx, unspecified site#N#170.9 Osteosarcoma#N#183.0 Ovary (ovarian)#N#157.9 Pancreas (pancreatic), unspecified part#N#163.8 Pleura/contiguous sites#N#185 Prostate#N#233.4 Prostate, in situ#N#154.1 Rectum#N#158.0 Retroperitoneum#N#171.9 Rhabdosarcoma#N#142.9 Salivary gland, unspecified site#N#171.9 Sarcoma, connective or soft tissue#N#172.9 Skin, melanoma, unspecified site#N#173.9 Skin, unspecified malignancy, unspecified site#N#151.9 Stomach, unspecified site#N#186.9 Testis (testicular), unspecified site#N#195.1 Thorax#N#193 Thyroid#N#141.9 Tongue, unspecified site#N#199.1 Unknown primary#N#179 Uterus (uterine), unspecified site.
207.00 Acute erythremia & erythroleukemia#N#207.00 Acute lymphoid leukemia (ALL)#N#206.00 Acute monocytic leukemia#N#205.00 Acyte myeloid leukemia (AML)#N#208.00 Acute leukemia, unspecified#N#277.30 E85.9 Amyloidosis#N#208.10 Chronic leukemia, unspecified#N#204.10 Chronic lymphoid leukemia (CLL)#N#206.10 Chronic monocytic leukemia#N#205.10 Chronic myeloid leukemia (CML)#N#202.40 Hairy cell leukemia#N#207.20 Megakaryocytic leukemia#N#273.1 D47.2 Monoclonal gammopathy of undetermined significance (MGUS)#N#203.00 C90.0 [0-2] Multiple myeloma (MM)#N#203.10 C90.1 [0-2] Plasma cell leukemia.
284.11 Antineoplastic chemotherapy induced pancytopenia#N#285.3 Antineoplastic chemotherapy induced anemia#N#995.29 Complication of chemotherapy#N#999.81 Extravasation of vesicant chemotherapy#N#V07.39 Need for other prophylactic chemotherapy#N#V58.11 Encounter for antineoplastic chemotherapy#N#V66.2 Convalescence following chemotherapy#N#V67.2 Follow-up examination following chemotherapy#N#V87.41 Personal history of antineoplastic chemotherapy.
Personal history of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism 1 Z86.2 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. 2 Short description: Prsnl history of dis of the bld/bld-form org/immun mechnsm 3 The 2021 edition of ICD-10-CM Z86.2 became effective on October 1, 2020. 4 This is the American ICD-10-CM version of Z86.2 - other international versions of ICD-10 Z86.2 may differ.
Personal history of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism 1 H/o: anemia 2 H/o: anemia - iron deficient 3 H/o: blood disorder 4 H/o: coagulation defect 5 History of anemia 6 History of aplastic anemia 7 History of autoimmune anemia 8 History of autoimmune hemolytic anemia 9 History of beta thalassemia 10 History of blood disease 11 History of coagulopathy (disorder of clotting) 12 History of disorder of the blood clotting system 13 History of histiocytosis 14 History of hypercoagulable state 15 History of hypercoagulable state (blood clots too easily) 16 History of immune disorder 17 History of iron deficiency 18 History of iron deficiency anemia 19 History of neutropenia 20 History of neutropenia (low white blood cell count) 21 History of other thrombocytopenia 22 History of sickle cell anemia 23 History of splenomegaly 24 History of splenomegaly (enlarged spleen) 25 History of thrombocytopenia (low platelet count) 26 Hx of anemia, other. 27 Hx of coagulopathy, other.