MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Anemia, Neonatal

(UMLS:C0002891)

Definition:: The mildest form of erythroblastosis fetalis in which anemia is the chief manifestation.
UMLS ID:: C0002891
MeSH ID:: D000751

Classification 1:

Name:

Hemic and Lymphatic Diseases
MeSH Tree Number(s):: C15.378.071.363

Classification 2:

Name:

Congenital, Hereditary, and Neonatal Diseases and Abnormalities
MeSH Tree Number(s):: C16.614.053

Synonym(s)

Anemia, Neonatal

ANAEMIA NEONATAL

ANEMIA NEONATAL

Anaemia neonatal

Neonatal anaemia

Neonatal anaemia, NOS

Neonatal anemia

Neonatal anemia, NOS

anaemia neonatal

10.

anemia neonatal

11.

anemia; newborn

12.

neonatal anaemia

13.

neonatal anemia

14.

newborn; anemia

Associated Drug(s)

	Name	Number of Reports	Reference(s)	Data Source
1	Mycophenolic Acid		17180133	CTD

Similar ADE(s)

	Name	Semantic Similarity
1	Anemia, Hemolytic	31.8%
2	Anemia, Macrocytic	31.8%
3	Anemia, Diamond-Blackfan	28.6%
4	Abdominal Cramps	27.9%
5	Amniotic Band Syndrome	27.9%
6	Asphyxia Neonatorum	27.9%
7	Infant, Premature, Diseases	27.9%
8	Infantile Colic	27.9%
9	Hemoglobinuria, Paroxysmal	25%
10	Disseminated Intravascular Coagulation	24.3%
11	Protein S Deficiency	24.3%
12	Anemia, Megaloblastic	23.6%
13	Anemia, Sickle Cell	23.1%
14	Thalassemia	23.1%
15	Thrombocythemia, Essential	22.4%
16	Thrombasthenia	21.8%
17	Antithrombin III Deficiency	21.8%
18	Protein C Deficiency	21.8%
19	Blood Coagulation Disorders	20.9%
20	Blood Platelet Disorders	20.9%
21	Bone Marrow Diseases	20.9%
22	Hemorrhagic Disorders	20.9%
23	Leukocyte Disorders	20.9%
24	Methemoglobinemia	20.9%
25	Pancytopenia	20.9%
26	Polycythemia	20.9%
27	Sulfhemoglobinemia	20.9%
28	Thrombophilia	20.9%
29	Erythrocytosis	20.9%
30	Persistent Fetal Circulation Syndrome	20.7%
31	Umbilical hernia	20.4%
32	Afibrinogenemia	20%
33	Factor VII Deficiency	20%
34	Factor X Deficiency	20%
35	Factor XII Deficiency	20%
36	Hemophilia A	20%
37	Activated Protein C Resistance	20%
38	Factor II deficiency	20%
39	Factor VIII Deficiency	20%
40	Factor V deficiency	20%
41	Factor XI Deficiency	20%
42	Hypoprothrombinemias	20%
43	Sickle Cell Trait	19%
44	Cystic Fibrosis	18.8%
45	Thrombocytosis	17.6%
46	Pelger-Huet Anomaly	17.2%
47	Fanconi Anemia	17.1%
48	Xeroderma	17%
49	Mobius Syndrome	17%
50	Neonatal Abstinence Syndrome	16.9%
51	Wiskott-Aldrich Syndrome	16.8%
52	Transfusion Reaction	16.4%
53	Hypotensive Transfusion Reaction	16.4%
54	Congenital nystagmus	16.3%
55	Bone Marrow Neoplasms	16.2%
56	Toxoplasmosis, Congenital	16.2%
57	Syphilis, Congenital	16.1%
58	Vitamin K Deficiency	16.1%
59	Meconium Aspiration Syndrome	15.8%
60	Pregnancy Complications, Hematologic	15.8%
61	Hematologic Neoplasms	15.8%
62	Hemolytic-Uremic Syndrome	15.6%
63	Paralysis, Obstetric	15.5%
64	Retinopathy of Prematurity	15.5%
65	Bronchopulmonary Dysplasia	15.1%
66	Leukemoid Reaction	15%
67	Polycythemia Vera	14.8%
68	Deformity	14.6%
69	Genetic Diseases, Inborn	14.6%
70	Acute Chest Syndrome	14.6%
71	Anemia, Pernicious	14.4%
72	Eosinophilia	13.6%
73	Hypoproteinemia	13.6%
74	Leukopenia	13.6%
75	Thrombocytopenia	13.6%
76	Leukostasis	13.6%
77	MYELODYSPLASTIC SYNDROME	13.6%
78	Congenital Hyperinsulinism	13.6%
79	Atypical Hemolytic Uremic Syndrome	13.1%
80	Kernicterus	12.7%
81	Respiratory Distress Syndrome, Newborn	12.5%
82	Lymphatic Abnormalities	12.3%
83	Purpura, Thrombotic Thrombocytopenic	12.3%
84	Lymphatic Diseases	12.2%
85	Beckwith-Wiedemann Syndrome	12.2%
86	Wolf-Hirschhorn Syndrome	12.2%
87	Ichthyosis, X-Linked	12%
88	Hydrops Fetalis	11.1%
89	Agammaglobulinemia	11%
90	Fetal Diseases	10.9%
91	Aicardi's syndrome	10.6%
92	Holoprosencephaly	10.4%
93	Leukocytosis	10.3%
94	Paraproteinemias	10.3%
95	Pleocytosis	10.3%
96	Smith-Magenis syndrome	10.2%
97	Primary Myelofibrosis	10.1%
98	Agranulocytosis	10.1%
99	Lymphocytosis	10.1%
100	Myelofibrosis	10.1%
101	Myeloid Metaplasia	10.1%
102	Hypoalbuminemia	10.1%
103	Hypereosinophilic syndrome	10.1%
104	bone marrow fibrosis	10.1%
105	Thrombotic Microangiopathies	10.1%
106	Chronic granulomatous disease	10.1%
107	Hyaline Membrane Disease	10.1%
108	Cri-du-Chat Syndrome	10.1%
109	Down Syndrome	10.1%
110	Trisomy 21	10.1%
111	Cryoglobulinemia	10%
112	Leukomalacia, Periventricular	10%
113	Monoclonal Gammopathy of Undetermined Significance	10%
114	Sjogren-Larsson Syndrome	10%
115	Hyperkeratosis, Epidermolytic	10%
116	Nesidioblastosis	9.9%
117	Ophthalmia Neonatorum	9.9%
118	Autoimmune thrombocytopenia	9.7%
119	Immune thrombocytopenic purpura	9.7%
120	CHARGE Syndrome	9.6%
121	Lymphangiectasis, Intestinal	9.5%
122	Fragile X Syndrome	9.4%
123	Abnormalities, Drug-Induced	9.3%
124	Situs Inversus	9.3%
125	Waldenstrom Macroglobulinemia	9.2%
126	Infectious Mononucleosis	8.9%
127	Heavy Chain Disease	8.7%
128	Ectodermal Dysplasia	8.7%
129	Aplasia Cutis Congenita	8.7%
130	Prader-Willi Syndrome	8.6%
131	Purpura, Hyperglobulinemic	8.5%
132	Rubinstein-Taybi Syndrome	8.5%
133	Neutropenia	8.4%
134	Hypergammaglobulinemia	8.3%
135	POEMS Syndrome	8.3%
136	Transfusion-Related Acute Lung Injury	8.2%
137	Ecchymosis	8.1%
138	Petechiae	8.1%
139	Purpura	8.1%
140	Nail-Patella Syndrome	8%
141	Thrombocytopenic purpura	8%
142	Kartagener Syndrome	7.9%
143	Pseudoxanthoma Elasticum	7.9%
144	Alstrom Syndrome	7.8%
145	Lymphopenia	7.7%
146	Job Syndrome	7.6%
147	Cockayne Syndrome	7.5%
148	Febrile Neutropenia	7.5%
149	Leukemia, Myelomonocytic, Chronic	7.5%
150	Multiple Myeloma	7.5%
151	Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative	7.5%
152	Anencephaly	7.4%
153	Eye Abnormalities	7.3%
154	Neoplastic Syndromes, Hereditary	7.3%
155	Cardiovascular Abnormalities	7.3%
156	Marfan Syndrome	7.2%
157	Skin Abnormalities	7%
158	Congenital Microtia	7%
159	Adenitis	7%
160	Histiocytosis	7%
161	Lymphadenitis	7%
162	Lymphangitis	7%
163	Lymphedema	7%
164	Splenic Diseases	7%
165	Thymus Hyperplasia	7%
166	Pseudolymphoma	7%
167	Lymphadenopathy	7%
168	Multiple Epiphyseal Dysplasia	6.9%
169	Osteochondrodysplasias	6.9%
170	Werner Syndrome	6.9%
171	Myasthenic Syndromes, Congenital	6.9%
172	Autoimmune Lymphoproliferative Syndrome	6.9%
173	Congenital diaphragmatic hernia	6.8%
174	Familial Mediterranean Fever	6.8%
175	Prune Belly Syndrome	6.8%
176	Twins, Conjoined	6.8%
177	Waardenburg Syndrome	6.8%
178	Muscular Dystrophy, Duchenne	6.6%
179	Polycystic Kidney Diseases	6.6%
180	Williams Syndrome	6.6%
181	Rett Syndrome	6.6%
182	Primary Ciliary Dyskinesia	6.6%
183	Smith-Lemli-Opitz Syndrome	6.6%
184	Classical Lissencephalies and Subcortical Band Heterotopias	6.4%
185	Pulmonary Eosinophilia	6.4%
186	Eosinophilic Pneumonia	6.4%
187	Albinism	6.3%
188	Waterhouse-Friderichsen Syndrome	6.2%
189	Maxillofacial Abnormalities	6.2%
190	Dural Arteriovenous Fistula	6.2%
191	Leukemia, Myeloid, Chronic-Phase	6.2%
192	Mucopolysaccharidosis II	6.2%
193	Dextrocardia	6.1%
194	Eosinophilia-Myalgia Syndrome	6.1%
195	Shwartzman Phenomenon	6%
196	Hemangioma, Cavernous	6%
197	Scurvy	6%
198	Purpura Fulminans	6%
199	Retinal Dysplasia	5.9%
200	Aniridia	5.9%
201	Urogenital Abnormalities	5.8%
202	Epidermolysis Bullosa	5.8%
203	Eosinophilic Granuloma	5.7%
204	Dwarfism	5.7%
205	Fetal Growth Retardation	5.5%
206	Polycystic Kidney, Autosomal Dominant	5.5%
207	Muscular Dystrophy	5.4%
208	Osteogenesis Imperfecta	5.4%
209	Fetal Hypoxia	5.4%
210	Fetal Alcohol Spectrum Disorders	5.4%
211	Menkes Kinky Hair Syndrome	5.4%
212	Lymphocele	5.3%
213	Lymphoproliferative Disorders	5.3%
214	Microcephaly	5.2%
215	Macrocephaly	5.2%
216	Kallmann Syndrome	5.2%
217	Anophthalmos	5.2%
218	Anus, Imperforate	5.2%
219	Hydranencephaly	5.2%
220	Microphthalmos	5.2%
221	Neural Tube Defects	5.2%
222	Tethered Cord Syndrome	5.2%
223	Iniencephaly	5.2%
224	Craniorachischisis	5.2%
225	Limb Deformities, Congenital	5.2%
226	Exencephaly	5.2%
227	Septo-Optic Dysplasia	5.2%
228	Craniofacial Abnormalities	5.2%
229	Cortical Dysplasia	5.2%
230	Malformations of Cortical Development	5.2%
231	Anorectal Malformations	5.2%
232	Thymus Neoplasms	5.2%
233	Tuberous Sclerosis	5.1%
234	Amino Acid Metabolism, Inborn Errors	5.1%
235	Bloom Syndrome	5.1%
236	Carbohydrate Metabolism, Inborn Errors	5.1%
237	Metal Metabolism, Inborn Errors	5.1%
238	Progeria	5.1%
239	Lysosomal Storage Diseases	5.1%
240	Cytochrome-c Oxidase Deficiency	5.1%
241	Peroxisomal Disorders	5.1%
242	Refsum Disease	5%
243	Turner Syndrome	5%
244	Neuronal Ceroid-Lipofuscinoses	5%
245	Porencephaly	4.9%
246	Klinefelter Syndrome	4.9%
247	Acrocephalosyndactylia	4.8%
248	Craniosynostosis	4.7%
249	Syndactyly	4.7%
250	Brachycephaly	4.7%
251	Scimitar Syndrome	4.7%
252	Charcot-Marie-Tooth Disease	4.7%
253	Antley-Bixler Syndrome Phenotype	4.7%
254	Elephantiasis	4.5%
255	Hypersplenism	4.5%
256	Sarcoidosis	4.5%
257	Elephantiasis Nostras Verrucosa	4.5%
258	Chorioamnionitis	4.5%
259	Angioedemas, Hereditary	4.5%
260	Myotonic Dystrophy	4.4%
261	Adrenoleukodystrophy	4.4%
262	Zellweger Syndrome	4.4%
263	Glycogen storage disease type II	4.4%
264	Fabry Disease	4.3%
265	Amelia	4.2%
266	Arachnodactyly	4.2%
267	Ectopia Cordis	4.2%
268	Ectromelia	4.2%
269	Hemimelia	4.2%
270	Meningomyelocele	4.2%
271	Noonan Syndrome	4.2%
272	Phocomelia	4.2%
273	Sirenomelia	4.2%
274	Spina Bifida	4.2%
275	Polydactyly	4.2%
276	Brachydactyly	4.2%
277	Plagiocephaly	4.2%
278	Lower Extremity Deformities, Congenital	4.2%
279	Upper Extremity Deformities, Congenital	4.2%
280	Single umbilical artery	4.2%
281	Poland Syndrome	4.2%
282	Mucopolysaccharidosis III	4.2%
283	Alkaptonuria	4.2%
284	Blepharophimosis	4.2%
285	Glycogen Storage Disease	4.2%
286	Hypophosphatasia	4.2%
287	Laryngostenosis	4.2%
288	Mouth Abnormalities	4.2%
289	Propionic acidemia	4.2%
290	Dihydropyrimidine Dehydrogenase Deficiency	4.2%
291	Cystinosis	4.2%
292	Cutis Laxa	4.1%
293	Esophageal Atresia	4.1%
294	Intestinal Atresia	4.1%
295	Mucocutaneous Lymph Node Syndrome	4.1%
296	Horseshoe Kidney	4.1%
297	Pectus excavatum	4.1%
298	Cleft Palate	4.1%
299	Galactosemias	4.1%
300	Urea Cycle Disorders, Inborn	4.1%
301	Tyrosinemias	4.1%
302	Klippel-Feil Syndrome	4.1%
303	Retinitis Pigmentosa	4.1%
304	Gastroschisis	4.1%
305	Synostosis	4.1%
306	Pigmentary retinopathy	4.1%
307	Hepatolenticular Degeneration	4.1%
308	Acrodermatitis	4.1%
309	Xeroderma Pigmentosum	4.1%
310	Porokeratosis	4.1%
311	Gianotti-Crosti Syndrome	4.1%
312	Keratoderma, Palmoplantar	4.1%
313	Amyloid Neuropathies, Familial	4%
314	Jaw Abnormalities	4%
315	Welander Distal Myopathy	4%
316	Niemann-Pick Disease, Type C	4%
317	Abnormalities, Radiation-Induced	3.8%
318	Dermal Sinus	3.7%
319	Spina Bifida Cystica	3.7%
320	Spina Bifida Occulta	3.7%
321	Lissencephaly	3.7%
322	Polymicrogyria	3.7%
323	Pachygyria	3.7%
324	Schizencephaly	3.7%
325	Periventricular Nodular Heterotopia	3.7%
326	Glycogen Storage Disease Type I	3.7%
327	Glycogen Storage Disease Type V	3.7%
328	Gaucher Disease	3.7%
329	Optic Atrophy, Hereditary, Leber	3.7%
330	Hyperphosphaturia	3.6%
331	Basal Cell Nevus Syndrome	3.6%
332	Micrognathism	3.6%
333	Pierre Robin Syndrome	3.6%
334	Tay-Sachs Disease	3.5%
335	Arthrogryposis	3.5%
336	Choanal Atresia	3.5%
337	Tracheobronchomegaly	3.5%
338	Laryngocele	3.5%
339	Homocystinuria	3.5%
340	Choledochal Cyst	3.4%
341	Duane Retraction Syndrome	3.4%
342	Granuloma	3.4%
343	Hermaphroditism	3.4%
344	Histiocytic Disorders, Malignant	3.4%
345	Leigh Disease	3.4%
346	Disorders of Sex Development	3.4%
347	Splenic Infarction	3.4%
348	Splenic Neoplasms	3.4%
349	Canavan Disease	3.4%
350	Alexander Disease	3.4%
351	Cryptorchidism	3.4%
352	Porphyrias, Hepatic	3.4%
353	Hypospadias	3.4%
354	Histiocytosis, Langerhans-Cell	3.4%
355	Tumor Lysis Syndrome	3.4%
356	Central Nervous System Cysts	3.4%
357	Dandy-Walker Syndrome	3.4%
358	Lymphohistiocytosis, Hemophagocytic	3.4%
359	Erdheim-Chester Disease	3.4%
360	Peutz-Jeghers Syndrome	3.4%
361	Aortic coarctation	3.4%
362	Cor Triatriatum	3.4%
363	Coronary Vessel Anomalies	3.4%
364	Dental Enamel Hypoplasia	3.4%
365	Patent ductus arteriosus	3.4%
366	Ebstein Anomaly	3.4%
367	Heart Septal Defects	3.4%
368	Hypodontia	3.4%
369	Macrostomia	3.4%
370	Meningocele	3.4%
371	Microstomia	3.4%
372	Tetralogy of Fallot	3.4%
373	Transposition of Great Vessels	3.4%
374	Hypoplastic Left Heart Syndrome	3.4%
375	May-Thurner Syndrome	3.4%
376	Encephalocele	3.4%
377	Myotonia Congenita	3.4%
378	Brain Diseases, Metabolic, Inborn	3.4%
379	Craniofacial Dysostosis	3.3%
380	Dystonia Musculorum Deformans	3.3%
381	Hypolipoproteinemias	3.3%
382	Papillon-Lefevre Disease	3.3%
383	Wolff-Parkinson-White Syndrome	3.3%
384	Lafora Disease	3.3%
385	Unverricht-Lundborg Syndrome	3.3%
386	Hyperlipidemia, Familial Combined	3.3%
387	Hyperlipoproteinemia Type III	3.3%
388	Carbamoyl-Phosphate Synthase I Deficiency Disease	3.2%
389	Retrognathia	3.2%
390	Ataxia Telangiectasia	3%
391	Aortopulmonary Septal Defect	3%
392	Double Outlet Right Ventricle	3%
393	Endocardial Cushion Defects	3%
394	Multiple Endocrine Neoplasia	3%
395	Laryngomalacia	3%
396	Myocardial bridging	3%
397	Aorticopulmonary Septal Defect	3%
398	Hypoalphalipoproteinemias	3%
399	Pectus carinatum	2.9%
400	Hyperandrogenism	2.9%
401	Bladder Exstrophy	2.9%
402	Congenital Hypothyroidism	2.9%
403	Epispadias	2.9%
404	Dermatitis, Atopic	2.9%
405	Prognathism	2.9%
406	Multicystic Dysplastic Kidney	2.9%
407	Sezary Syndrome	2.9%
408	Familial Periodic Paralysis	2.8%
409	Long QT Syndrome	2.8%
410	Platybasia	2.8%
411	Tricuspid Atresia	2.8%
412	Arrhythmogenic Right Ventricular Dysplasia	2.8%
413	Truncus Arteriosus, Persistent	2.8%
414	Gonadal Dysgenesis	2.8%
415	Splenic Rupture	2.8%
416	Bronchomalacia	2.8%
417	Goldenhar Syndrome	2.8%
418	Adrenogenital Syndrome	2.8%
419	Tracheomalacia	2.8%
420	Ovotesticular Disorders of Sex Development	2.8%
421	Lactose Intolerance	2.8%
422	Variegate Porphyria	2.8%
423	Acute intermittent porphyria	2.8%
424	Porphyria Cutanea Tarda	2.8%
425	Hyperhomocysteinemia	2.8%
426	Renal Aminoacidurias	2.7%
427	Fanconi Syndrome	2.7%
428	Lymphoma	2.7%
429	Pseudohypoaldosteronism	2.7%
430	Liddle Syndrome	2.7%
431	Hyperlipoproteinemia Type IV	2.7%
432	Hyperlipoproteinemia Type V	2.7%
433	Thymoma	2.7%
434	Malignant histiocytosis	2.5%
435	Sarcoidosis, Pulmonary	2.5%
436	Histiocytic sarcoma	2.5%
437	Behcet Syndrome	2.5%
438	Hypokalemic periodic paralysis	2.5%
439	Mandibulofacial Dysostosis	2.5%
440	Romano-Ward Syndrome	2.5%
441	Cystinuria	2.4%
442	Gout	2.4%
443	Multiple Endocrine Neoplasia Type 1	2.4%
444	Pseudohypoparathyroidism	2.4%
445	Friedreich Ataxia	2.4%
446	Talipes	2.3%
447	Renal tubular acidosis	2.3%
448	Congenital clubfoot	2.2%
449	Vertical Talus	2.2%
450	Huntington Disease	2.2%
451	Denys-Drash Syndrome	2.2%
452	Arthritis, Gouty	2.1%
453	Familial Hypophosphatemic Rickets	2.1%
454	Splenosis	2%
455	Hodgkin Disease	2%
456	Lymphoma, Non-Hodgkin	2%
457	Leukemia, T-Cell	2%
458	Leukemia, B-Cell	2%
459	Nephroblastoma	2%
460	Arteriovenous fistula	1.9%
461	Glycosuria, Renal	1.8%
462	Adenomatous Polyposis Coli	1.8%
463	Composite Lymphoma	1.7%
464	Lymphangioleiomyomatosis	1.6%
465	Lymphoma, Follicular	1.6%
466	T-Cell Lymphoma	1.6%
467	Mantle cell lymphoma	1.6%
468	Precursor B-Cell Lymphoblastic Leukemia-Lymphoma	1.6%
469	Leukemia, Large Granular Lymphocytic	1.6%
470	Precursor T-Cell Lymphoblastic Leukemia-Lymphoma	1.6%
471	MELAS Syndrome	1.5%
472	Lymphoma, T-Cell, Cutaneous	1.5%
473	Lymphoma, AIDS-Related	1.5%
474	Enteropathy-Associated T-Cell Lymphoma	1.5%
475	Primary Effusion Lymphoma	1.5%
476	Mycosis Fungoides	1.4%
477	Lymphomatoid Papulosis	1.4%
478	Plasmablastic lymphoma	1.4%
479	Lymphomatoid Granulomatosis	1.2%
480	Burkitt Lymphoma	1.1%

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