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>> Disorder Abbreviations
Look through 177 acronyms and abbreviations related to Disorder:
CF
— Cystic Fibrosis
CCM
— Cerebral Cavernous Malformation
CHF
— Congestive Heart Failure
CGI
— Clinical Global Impression
CIN
— Conjunctival Intraepithelial Neoplasia
CLD
— Chronic Liver Disease
SIDS
— Sudden Infant Death Syndrome
FICP
— Fatal Infantile Cardiomyopathy Plus
CCHS
— Congenital central hypoventilation syndrome
CIN
— Cervical Intraepithelial Neoplasia
CGD
— Chronic Granulomatous Disease
CIDP
— Chronic inflammatory demyelinating polyneuropathy
PD
— Parkinson's Disease
CHD
— Coronary Heart Disease
AD
— Alzheimer's Disease
DSH
— Deliberate Self-Harm
CML
— Chronic Myeloid Leukemia
CCD
— Classic Cleidocranial Dysplasia
CLD
— Chronic Lung Disease
CH
— Chronic Hepatitis
CID
— Combined Immunodeficiency Disease
CGAP
— Cancer Genome Anatomy Project
CIS
— Carcinoma in Situ
CCM
— Cerebral Capillary Malformation
CLAH
— Congenital Lipoid Adrenal Hyperplasia
CEL
— Chronic Eosinophilic Leukemia
CHD
— Congenital Heart Disease
CD
— Celiac Disease
MERRF
— Myoclonic Epilepsy and Ragged Red Muscle Fibers
CHA
— Congenital Hypoplastic Anemia
CPEO
— Chronic Progressive External Ophthalmoplegia
CME
— Cystoid Macular Edema
SNHL
— Sensorineural Hearing Loss
CDH
— Congenital Diaphragmatic Hernia
CHL
— Classic Hodgkin Lymphoma
MELAS
— Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-like episodes
CLH
— Cutaneous Lymphoid Hyperplasia
CGL
— Chronic Granulocytic Leukemia
CGL
— Congenital Generalized Lipodystrophy
CHR
— complete hematologic response
CHB
— congenital heart block
CLL
— Chronic Lymphoid Leukaemia
CD
— Conduct Disorder
CLD
— combined lipase deficiency
ANT
— Adenine Nucleotide Translocator
CCS
— clear cell sarcoma
CHB
— Chronic Hepatitis B
CEPH
— Centre Etude Polymorphism Humain
DIDMOAD
— Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, Deafness
CEP
— Congenital Erythropoietic Porphyria
CMD
— Cartilage Matrix Deficiency
CDLS
— Cornelia De Lange Syndrome
CHR
— Complete Hematologic Remission
CFTD
— Congenital Fiber-Type Disproportion
CCRCC
— Clear Cell Renal Cell Carcinoma
MDM
— Myopathy and Diabetes Mellitus
CH
— congenital hypothyroidism
CCHB
— Complete Congenital Heart Block
CDA
— congenital dyserythropoietic anemia
CH
— cystic hygroma
CH
— Cluster Headache
CIIP
— Chronic Idiopathic Intestinal Pseudoobstruction
CES
— Cat Eye Syndrome
CL
— Cleft Lip
CIN
— Chronic Idiopathic Neutropenia
CHED
— Congenital Heredity Endothelial Dystrophy
CLD
— Congenital Lactase Deficiency
CGH
— Congenital Generalized Hypertrichosis
CM
— complete mole
CD
— Coeliac Disease
CI
— Cerebral Infarction
CIBD
— Chronic Inflammatory Bowel Disease
PDH
— Pyruvate DeHydrogenase
CISS
— Chromosome Instability Syndromes
CFS
— Cancer Family Syndrome
CD
— cortical dysplasia
CLD
— Cholestatic Liver Disease
PEO
— PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA
CCFDN
— Congenital cataracts facial dysmorphism neuropathy
CESD
— Cholesterol Ester Storage Disease
CFF
— Cystic Fibrosis Factor
PEM
— Progressive Encephalopathy
CIPO
— Chronic Intestinal Pseudoobstruction with myopathy and Ophthalmoplegia
CDCS
— Cri Du Chat Syndrome
NARP
— neurogenic muscle weakness, ataxia and retinitis pigmentosa
CMD
— Congenital Myotonic Dystrophy
CM
— Capillary malformation
CHD
— Congenital Heart Defect
CM
— cutaneous melanoma
FBSN
— Familial Bilateral Striatal Necrosis
CEA
— Collie Eye Anomaly
CL
— cystic lymphangioma
CGKD
— Complex Glycerol Kinase Deficiency
CDC
— Collecting duct carcinoma
CH
— congenital hydrocephalus
CLD
— Chronic Lymphoproliferative Disorder
CID
— Combined Immune Deficiency
CML
— Chronic Myelogenic Leukemia
ADPD
— Alzheimer's Disease and Parkinsons's Disease
CM
— Cardiac Myxoma
CD
— Cowden Disease
PME
— Progressive Myoclonus Epilepsy
CM
— Congenital Malformations
CIPD
— Chronic Inflammatory Proliferative Diseases
CD
— Congenital Defects
MEPR
— Myoclonic Epilepsy and Psychomotor Regression
CI
— Coccidioides immitis
AMDF
— Ataxia, Myoclonus and Deafness
CD
— Campomelic dysplasia
MICM
— Maternally Inherited Cardiomyopathy
CD
— Crohn disease
MMC
— Maternal Myopathy and Cardiomyopathy
CD
— Canavan disease
CD
— Cone Degeneration
CI
— cardiac involvement
KSS
— Keams Sayre Syndrome
ESOC
— Epilepsy, Strokes, Optic atrophy and Cognitive decline
MNGIE
— Myopathy and external ophthalmoplegia, Neuropathy, Gastro-Intestinal, Encephalopathy
DMDF
— Diabetes Mellitus and Deafness
MHCM
— Maternally Inherited Hypertrophic CardioMyopathy
CCM
— Congenital Cardiovascular Malformation
CML
— cutaneous malignant lymphomas
MM
— Mitochondrial myopathy
MILS
— Maternally Inherited Leigh Syndrome
DEMCHO
— Dementia and Chorea
LHON
— Leber Hereditary Optic Neuropathy
LDYT
— Leber's hereditary optic neuropathy and DYsTonia
LEVIM
— Lethal Infantile Mitochondrial Myopathy
CHDH
— Congenital Heart Disease History
CGVHD
— Chronic Graft Versus Host Disease
CHDS
— Conotruncal Heart Defects
SI
— Self-Injury
CHC
— Chronic Hepatitis C
PMPS
— Pearson Marrow-Pancreas Syndrome
CM
— Clinically Malignant
CMGM
— chronic megakaryocytic granulocytic metaplasia
CDS
— Caudal Dysplasia Sequence
CEST
— Childhood Endodermal Sinus Tumors
CDDS
— Congenital Diaphragmatic Defects
CE
— Coelomic Epithelium
CHM
— Congenital Heart Malformation
CMGM
— Chronic Megakaryocytic Granulocytic Myelosis
CLI
— Central Lymphatic Irradiation
CEMA
— Chronic enteroviral meningoencephalitis with agammaglobulinemia
CMD
— Chronic Myeloproliferative Disorders
CFS
— congenital fibrosis syndromes
CCRC
— Clear Cell Renal Carcinoma
CDD
— Congenital Developmental Defects
CMCA
— Clonal Marrow Cytogenetic Abnormalities
CMD
— Chronic Myeloid Disorders
CHDS
— Congenital Heart Disorders
CCW
— cataract and curly whiskers
CHI
— Congenital Hydrocephalus Internus
SH
— Self-Harm
CHN
— Chinese Herb Nephropathy
CCRC
— Chromophobe Cell Renal Carcinoma
CIPA
— Carcinomas In Pleomorphic Adenoma
CMC
— Chronic Mucocutaneous Candidiases
CGL
— Candidate Gene Loci
CF
— Chondromyxoid Fibroma
CCAS
— Complex Chromosomal Abnormalities
CCOF
— Chromosome Competent Ovarian Failure
RBD
— Rare Bleeding Disorders
CH
— Congenital Hydronephrosis
SIB
— Self-injurious behaviour
CLP
— Cleft lip palates
CH
— Cerebellar Hemangioblastoma
CK
— Cervical Keratinocytes
CL
— Congenital Leukaemia
CL
— Cirrhotic Liver
CM
— Coloboma Mutation
CD
— Chromosomal Damage
CCA
— Constitutional Chromosome Abnormalities
SIV
— Self-Inflicted Violence
CML
— Chronic Myeloctyic Leukemia
CD
— Chromosome Damage
PDH
— anti-pyruvate dehydrogenase
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