-- Muscle Deficiency
Q79.4
- Abstinence, Neonatal
P96.1
- Acid Pulmonary Aspiration, Obstetric
O74.0
-- Congenital, Associated With Enzyme Deficiency
E25.0
- Alveolar Hypoventilation
E66.2
- Alveolocapillary Block
J84.10
- Ankyloglossia Superior
Q38.1
---- Cervicothoracic Region
M47.013
---- Occipito-atlanto-axial Region
M47.011
- Antidepressant Discontinuation
T43.205
- Aortomesenteric Duodenum Occlusion
K31.5
- Argentaffin, Argintaffinoma
E34.0
- Ataxia-telangiectasia
G11.3
- Autoerythrocyte Sensitization
D69.2
- Autoimmune Polyglandular
E31.0
- Autoimmune Lymphoproliferative [ALPS]
D89.82
-- Specified Type NEC
M04.8
- Barsony-Teschendorf
K22.4
- Bilateral Polycystic Ovarian
E28.2
- Birt-Hogg-Dube Syndrome
Q87.89
- Bradycardia-tachycardia
I49.5
-- With Psychosis, Psychotic Reaction
F09
-- Personality Change
F07.0
-- Postcontusional
F07.81
-- Post-traumatic, Nonpsychotic
F07.81
- Brain Stem Stroke
G46.3
- Broad Ligament Laceration
N83.8
- Carbohydrate-deficient Glycoprotein
E77.8
- Carcinogenic Thrombophlebitis
I82.1
- Cardiopulmonary-obesity
E66.2
- Cardiorespiratory Distress, Newborn
P22.0
-- Artery Compression
I77.4
-- Posterior, Sympathicus
M53.0
-- Sympathetic Paralysis
G90.2
- Cervicodorsal Outlet
G54.2
- Cervicothoracic Outlet
G54.0
- Chondrocostal Junction
M94.0
- Chondroectodermal Dysplasia
Q77.6
- Chromosome 4 Short Arm Deletion
Q93.3
- Chromosome 5 Short Arm Deletion
Q93.4
-- Infantile Neurological, Cutaneous And Articular
M04.2
- Clerambault's Automatism
G93.89
- Clumsiness, Clumsy Child
F82
- Combined Immunity Deficiency
D81.9
--- Occipito-atlanto-axial Region
M47.021
-- Affecting Multiple Systems NEC
Q87.89
-- Central Alveolar Hypoventilation
G47.35
-- Muscular Hypertrophy-cerebral
Q87.89
-- Oculo-auriculovertebral
Q87.0
-- Oculofacial Diplegia
Q87.0
- Congestion-fibrosis, Female
N94.89
- Congestive Dysmenorrhea
N94.6
- Costochondral Junction
M94.0
--- Alcohol
--- Overproduction Of Pituitary ACTH
E24.0
-- Pituitary-dependent
E24.0
-- Specified Type NEC
E24.8
- Cryopyrin-associated Periodic
M04.2
- Cystic Duct Stump
K91.5
- Depersonalization
F48.1
- Diabetes Mellitus In Newborn Infant
P70.2
- Döhle Body-panmyelopathic
D72.0
- Dorsolateral Medullary
G46.4
-- Without Status Epilepticus
G40.834
- Drug Withdrawal, Infant Of Dependent Mother
P96.1
---- Female Phenotype
Q97.9
---- Male Phenotype
Q98.9
- Dyspraxia, Developmental
F82
- Eczema-thrombocytopenia
D82.0
- Ellis-van Creveld
Q77.6
- Endocrine-hypertensive
E27.0
- Eosinophilia-myalgia
M35.8
---- With Status Epilepticus
G40.A11
---- Without Status Epilepticus
G40.A19
---- With Status Epilepticus
G40.A01
---- Without Status Epilepticus
G40.A09
- Erythrocyte Fragmentation
D59.4
- Eyelid-malar-mandible
Q87.0
- Facial Pain, Paroxysmal
G50.0
- Familial Cold Autoinflammatory
M04.2
- Familial Eczema-thrombocytopenia
D82.0
--- Chlamydia Trachomatis
A74.81
--- Neisseria Gonorrhorea
A54.85
- Food Protein-induced Enterocolitis
K52.21
-- Auriculotemporal
G50.8
- Friderichsen-Waterhouse
A39.1
-- Prepubertal Castrate
E29.1
-- Laceration-hemorrhage
K22.6
- Gastrojejunal Loop Obstruction
K91.89
- Gee-Herter-Heubner
K90.0
- Gerstmann-Sträussler-Scheinker
A81.82
- Gilles De La Tourette's
F95.2
- Gustatory Sweating
G50.8
- Hemophagocytic, Infection-associated
D76.2
-- Following Delivery
O90.4
-- Postoperative Or Postprocedural
K91.83
-- Postpartum, Puerperal
O90.4
- Histiocytosis NEC
D76.3
- HIV Infection, Acute
B20
- Hunterian Glossitis
D51.0
- Hyperammonemia-hyperornithinemia-homocitrullinemia
E72.4
- Hyperimmunoglobulin D
M04.1
- Hyperimmunoglobulin E
D82.4
- Hypertransfusion, Newborn
P61.1
- Hypoplastic Left-heart
Q23.4
- Hypotension, Maternal
O26.5-
- Hypoventilation, Obesity
E66.2
-- Cardiorespiratory Distress, Newborn
P22.0
- Immobility, Immobilization
M62.3
- Immune Reconstitution
D89.3
- Immune Reconstitution Inflammatory [IRIS]
D89.3
- Immunity Deficiency, Combined
D81.9
- Impending Coronary
I20.0
- Impingement, Shoulder
M75.4-
- Inappropriate Secretion Of Antidiuretic Hormone
E22.2
-- Of Diabetic Mother
P70.1
-- Gestational Diabetes
P70.0
- Inferior Vena Cava
I87.1
- Intravascular Coagulation-fibrinolysis
D65
--- Due To Mesenteric Artery Insufficiency
K55.1
- Jervell-Lange-Nielsen
I45.81
- Joseph-Diamond-Blackfan
D61.01
- Krabbe's Congenital Muscle Hypoplasia
Q79.8
--- Neoplastic Disease
G73.1
--- Specified Disease NEC
G70.81
-- Cutaneous Nerve Of Thigh
G57.1-
--- With Status Epilepticus
G40.813
--- Without Status Epilepticus
G40.814
--- With Status Epilepticus
G40.811
--- Without Status Epilepticus
G40.812
- Lenticular, Progressive
E83.01
- Limbic Epilepsy Personality
F07.0
- Long Arm 18 Or 21 Deletion
Q93.89
-- Atmospheric Pressure
T70.29
- Lower Radicular, Newborn
P14.8
-- Due To Infection
D76.2
- Magnesium-deficiency
R29.0
- Mal De Debarquement
R42
-- Exogenous Cause NEC
Q86.8
- Mandibulofacial Dysostosis
Q75.4
- Maple-syrup-urine
E71.0
--- Ocular Manifestations
Q87.42
--- Skeletal Manifestations
Q87.43
- Meekeren-Ehlers-Danlos
Q79.6
-- Vascular Insufficiency
K55.1
- Micrognathia-glossoptosis
Q87.0
- Minkowski-Chauffard
D58.0
- Morgagni-Adams-Stokes
I45.9
- Mucocutaneous Lymph Node
M30.3
---- Lower Respiratory Infection
J47.0
----- Lower Respiratory Infection
J47.0
--- Isolated Del Chromosomal Abnormality
D46.C
---- With Ringed Sideroblasts
D46.B
- Myeloid Hypereosinophilic
D72.118
- Myeloproliferative
D47.1
- Neonatal Abstinence
P96.1
-- Rapidly Progressive
N01.9
---- Glomerulonephritis
N04.A
----- With Dense Deposit Disease
N04.6
--- Dense Deposit Disease
N04.6
---- Crescentic Glomerulonephritis
N04.7
---- Endocapillary Proliferative Glomerulonephritis
N04.4
---- Membranous Glomerulonephritis
N04.2
---- Mesangial Proliferative Glomerulonephritis
N04.3
---- Mesangiocapillary Glomerulonephritis
N04.5
--- Focal And Segmental Glomerular Lesions
N04.1
--- Minor Glomerular Abnormality
N04.0
--- Specified Morphological Changes NEC
N04.8
- Neurologic Neglect
R41.4
- Nonne-Milroy-Meige
Q82.0
- Nothnagel's Vasomotor Acroparesthesia
I73.89
- Obesity Hypoventilation
E66.2
- Oral-facial-digital
Q87.0
- Oro-facial-digital
Q87.0
- Osler-Weber-Rendu
I78.0
- Osteoporosis-osteomalacia
M83.8
- Osterreicher-Turner
Q87.2
- Oto-palatal-digital
Q87.0
- Paget-Schroetter
I82.890
- Paroxysmal Facial Pain
G50.0
- Pediatric Autoimmune Neuropsychiatric Disorders Associated With Streptococcal Infections
D89.89
- Pellagra-cerebellar Ataxia-renal Aminoaciduria
E72.02
- Pelvic Congestion-fibrosis, Female
N94.89
- Periodic Fever, Aphthous Stomatitis, Pharyngitis, And Adenopathy [PFAPA]
M04.8
- Periurethral Fibrosis
N13.5
- Pigmentary Pallidal Degeneration
G23.0
- Pluricarential Of Infancy
E40
- Polyangiitis Overlap
M30.8
- Polycarential Of Infancy
E40
-- Postmyocardial Infarction
I24.1
- Post Chemoembolization - Code To Associated Conditions
- Postcholecystectomy
K91.5
- Postcommissurotomy
I97.0
- Postconcussional
F07.81
- Postencephalitic
F07.89
- Post Endometrial Ablation
N99.85
-- Cervical Sympathetic
M53.0
-- Fossa Compression
G93.5
-- Reversible Encephalopathy
I67.83
- Postgastric Surgery
K91.1
- Postlaminectomy NEC
M96.1
- Postmastectomy Lymphedema
I97.2
- Postmyocardial Infarction
I24.1
- Postpartum Panhypopituitary
E23.0
--- Specified Complication NEC
I87.09-
- Potassium Intoxication
E87.5
- Precerebral Artery
G45.2
- Premature Senility
E34.8
- Premenstrual Dysphoric
F32.81
- Premenstrual Tension
N94.3
-- Hallucinatory Type
F06.0
-- Nonpsychotic Severity
F07.0
-- Arteriosclerosis
I27.0
- Pyogenic Arthritis, Pyoderma Gangrenosum, And Acne [PAPA]
M04.8
- Pyramidopallidonigral
G20
- QT Interval Prolongation
I45.81
-- Upper Limbs, Newborn
P14.3
- Rapid Time-zone Change
G47.25
- Reactive Airways Dysfunction
J68.3
- Rendu-Osler-Weber
I78.0
- Retroperitoneal Fibrosis
N13.5
- Retroviral Seroconversion
Z21
-- Heart, Hypoplastic
Q22.6
---- Causing Heat Exhaustion Or Prostration
T67.4
- Scaglietti-Dagnini
E22.0
- Schizophrenic, Of Childhood NEC
F84.5
- Schüller-Christian
C96.5
- Sclerocystic Ovary
E28.2
- Septicemic Adrenal Hemorrhage
A39.1
- Seroconversion, Retroviral
Z21
- Serous Meningitis
G93.2
- Severe Acute Respiratory
J12.81
--- Following Crush Injury
T79.5
- Shone's - Code To Specific Anomalies
- Siemens' Ectodermal Dysplasia
Q82.4
- Sinusitis-bronchiectasis-situs Inversus
Q89.3
- Slow Flow, Coronary
I20.8
- Sneddon-Wilkinson
L13.1
- South African Cardiomyopathy
I42.8
-- Upward Movement, Eyes
H51.8
- Staphylococcal Scalded Skin
L00
-- Toxic Epidermal Necrolysis Overlap
L51.3
- Straight Back, Congenital
Q76.49
- Subcoracoid-pectoralis Minor
G54.0
- Subcostal Nerve Compression
I77.89
- Subphrenic Interposition
Q43.3
-- Mesenteric Artery
K55.1
-- Semi-circular Canal Dehiscence
H83.8X-
- Suprarenal Cortical
E27.0
-- Cervical Paralysis
G90.2
-- With Acute Organ Dysfunction
R65.11
- Tachycardia-bradycardia
I49.5
- Telangiectasic-pigmentation-cataract
Q82.8
- Temporomandibular Joint-pain-dysfunction
M26.62-
- Testicular Feminization
E34.51
- Thrombocytopenia With Absent Radius
Q87.2
- Thyroid-adrenocortical Insufficiency
E31.0
- Transient Left Ventricular Apical Ballooning
I51.81
- Traumatic Vasospastic
T75.22
--- Meiotic Nondisjunction
Q91.4
--- Mitotic Nondisjunction
Q91.5
--- Meiotic Nondisjunction
Q91.0
--- Mitotic Nondisjunction
Q91.1
--- Meiotic Nondisjunction
Q90.0
--- Mitotic Nondisjunction
Q90.1
- Tumor Necrosis Factor Receptor Associated Periodic
M04.1
-- Automatic Implantable Defibrillator
T82.198
- Vascular NEC In Cerebrovascular Disease
G46.8
- Vasoconstriction, Reversible Cerebrovascular
I67.841
- Vertebro-basilar Artery
G45.0
- Visceral Larva Migrans
B83.0
- Visual Disorientation
H53.8
- Vitamin B6 Deficiency
E53.1
- Waldenström-Kjellberg
D50.1
---- With Kidney Involvement
M31.31
- Wilkinson-Sneddon
L13.1
--- Infant Of Dependent Mother
P96.1
--- Therapeutic Use, Newborn
P96.2