MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Pseudohypoparathyroidism

(UMLS:C0033806)

Definition:: A hereditary syndrome clinically similar to HYPOPARATHYROIDISM. It is characterized by HYPOCALCEMIA; HYPERPHOSPHATEMIA; and associated skeletal development impairment and caused by failure of response to PARATHYROID HORMONE rather than deficiencies. A severe form with resistance to multiple hormones is referred to as Type 1a and is associated with maternal mutant allele of the ALPHA CHAIN OF STIMULATORY G PROTEIN.
UMLS ID:: C0033806
MeSH ID:: D011547

Classification 1:

Name:

Musculoskeletal Diseases
MeSH Tree Number(s):: C05.116.198.709

Classification 2:

Name:

Congenital, Hereditary, and Neonatal Diseases and Abnormalities
MeSH Tree Number(s):: C16.320.565.618.815

Classification 3:

Name:

Nutritional and Metabolic Diseases
MeSH Tree Number(s):: C18.452.104.709|C18.452.174.766|C18.452.648.618.815

Synonym(s)

Pseudohypoparathyroidism

AHO - Albright hereditary osteodystrophy

Albright hereditary osteodystrophy

Albright hereditary osteodystrophy (AHO)

Albright hereditary osteodystrophy, NOS

Albright syndrome 1

Constitutional chronic hypocalcaemia

Constitutional chronic hypocalcemia

Familial pseudohypoparathyroidism

10.

Fuller Albright syndrome 1

11.

MARTIN-ALBRIGHT SYNDROME

12.

PHP - Pseudohypoparathyroidism

13.

PSEUDOHYPOPARATHYROIDISM

14.

Parathyroid hormone resistant hypoparathyroidism

15.

Pseudo-hypoparathyroidism

Associated Drug(s)

	Name	Number of Reports	Reference(s)	Data Source
1	Calcitriol	FAERS: 1	2856045 6688127	CTD US FAERS
2	Calcium Gluconate	FAERS: 1		US FAERS
3	Cinacalcet	FAERS: 1		US FAERS
4	Thyroxine	FAERS: 1		US FAERS
5	Valproic Acid	FAERS: 1		US FAERS

Similar ADE(s)

	Name	Semantic Similarity
1	Rickets	48.1%
2	Familial Hypophosphatemic Rickets	40.8%
3	Hyperphosphaturia	40.1%
4	Hypercalcemia	38.7%
5	Hypocalcemia	38.7%
6	Milk-Alkali Syndrome	38.7%
7	Leigh Disease	37.6%
8	Hypophosphatasia	36.4%
9	Osteoporosis	36.3%
10	Bone Demineralization, Pathologic	36.3%
11	Post-Traumatic Osteoporosis	36.3%
12	Brain Diseases, Metabolic, Inborn	36.3%
13	Osteomalacia	35.5%
14	Smith-Lemli-Opitz Syndrome	35.3%
15	Menkes Kinky Hair Syndrome	34.6%
16	Galactosemias	34.3%
17	Urea Cycle Disorders, Inborn	34.3%
18	Tyrosinemias	34.3%
19	Carbamoyl-Phosphate Synthase I Deficiency Disease	33.5%
20	Wasting Syndrome	32.7%
21	Hepatolenticular Degeneration	32.2%
22	Glycogen storage disease type II	31.5%
23	Amino Acid Metabolism, Inborn Errors	31.1%
24	Carbohydrate Metabolism, Inborn Errors	31.1%
25	Progeria	31.1%
26	Lysosomal Storage Diseases	31.1%
27	Peroxisomal Disorders	31.1%
28	Familial Periodic Paralysis	30.9%
29	Hyperhomocysteinemia	30.7%
30	Gaucher Disease	29.6%
31	Hyperlipoproteinemia Type IV	29%
32	Hyperlipoproteinemia Type V	29%
33	Homocystinuria	28.8%
34	Lactose Intolerance	28.7%
35	Hypolipoproteinemias	28.6%
36	Acid-Base Imbalance	28.3%
37	Iron Metabolism Disorders	28.3%
38	Phosphorus Metabolism Disorders	28.3%
39	Water-Electrolyte Imbalance	28.3%
40	Lipid Metabolism Disorders	28.3%
41	Mitochondrial Diseases	28.3%
42	Glucose Metabolism Disorders	28.3%
43	Adrenoleukodystrophy	28.2%
44	Lipodystrophy	27.3%
45	Calcinosis	26.9%
46	Hyperlipidemia, Familial Combined	26.7%
47	Renal Osteodystrophy	26.7%
48	Renal rickets	26.7%
49	Osteoporosis, Postmenopausal	26.6%
50	Fabry Disease	26.2%
51	Zellweger Syndrome	26%
52	Tay-Sachs Disease	25.8%
53	Hyperlipoproteinemia Type III	25.7%
54	Amyloid Neuropathies, Familial	25.5%
55	Cytochrome-c Oxidase Deficiency	25.5%
56	Niemann-Pick Disease, Type C	25.3%
57	Refsum Disease	25.2%
58	Brain Diseases, Metabolic	24.3%
59	Mucopolysaccharidosis III	23.3%
60	Hypokalemic periodic paralysis	23.2%
61	Werner Syndrome	22.9%
62	Renal tubular acidosis	22.8%
63	Neuronal Ceroid-Lipofuscinoses	22.5%
64	Hypoalphalipoproteinemias	22.5%
65	Alkaptonuria	21.5%
66	Glycogen Storage Disease	21.5%
67	Propionic acidemia	21.5%
68	Dihydropyrimidine Dehydrogenase Deficiency	21.5%
69	Cystinosis	21.5%
70	MELAS Syndrome	21.4%
71	Mucopolysaccharidosis II	20.9%
72	Mitochondrial Encephalomyopathies	20%
73	Gout	19.9%
74	Pseudohypoparathyroidism	19.7%
75	Calciphylaxis	19.7%
76	Vascular calcification	19.7%
77	Congenital Hyperinsulinism	19.6%
78	Antley-Bixler Syndrome Phenotype	19.4%
79	Cockayne Syndrome	18.9%
80	Glycosuria, Renal	18.9%
81	Calcium Metabolism Disorders	18.3%
82	Acidosis	18.1%
83	Alkalosis	18.1%
84	Amyloidosis	18.1%
85	Hyperglycemia	18.1%
86	Hyperinsulinism	18.1%
87	Hyperkalemia	18.1%
88	Hypernatremia	18.1%
89	Hypoglycemia	18.1%
90	Hypokalemia	18.1%
91	Hyponatremia	18.1%
92	Xanthomatosis	18.1%
93	Hypophosphatemia	18.1%
94	Metabolic acidosis	18.1%
95	Dyslipidemias	18.1%
96	Iron Overload	18.1%
97	Xanthoma	18.1%
98	Diabetic Ketoacidosis	17.8%
99	Albinism	17.6%
100	Sjogren-Larsson Syndrome	17.2%
101	Bloom Syndrome	17%
102	Glycogen Storage Disease Type I	16.7%
103	Glycogen Storage Disease Type V	16.7%
104	Renal Aminoacidurias	16.6%
105	Fanconi Syndrome	16.6%
106	Pseudohypoaldosteronism	16.6%
107	Liddle Syndrome	16.6%
108	Nutrition Disorders	16.5%
109	Mitochondrial Myopathies	16.3%
110	Ichthyosis, X-Linked	16.2%
111	Canavan Disease	16.1%
112	Alexander Disease	16.1%
113	Diabetes Mellitus	16%
114	Osteopenia	15.9%
115	Dehydration	15.7%
116	Lipomatosis	15.7%
117	Water Intoxication	15.7%
118	Achlorhydria	15.6%
119	Porphyrias, Hepatic	15.6%
120	Celiac Disease	15.5%
121	Sprue, Tropical	15.5%
122	Steatorrhea	15.5%
123	Sprue	15.5%
124	Fanconi Anemia	15.3%
125	Nesidioblastosis	15.3%
126	Arthritis, Gouty	15%
127	Nephrocalcinosis	14.8%
128	Tetany	14.8%
129	HIV Wasting Syndrome	14.4%
130	HIV-Associated Lipodystrophy Syndrome	14.2%
131	Myelinolysis, Central Pontine	13.7%
132	Glycosuria	13.6%
133	Reye Syndrome	13.6%
134	Hepatic Encephalopathy	13.5%
135	Ataxia Telangiectasia	13.4%
136	Acidosis, Lactic	13.1%
137	Hemosiderosis	13.1%
138	Ketosis	13.1%
139	Ketonuria	13.1%
140	Ketoacidosis	13.1%
141	Ketonemia	13.1%
142	Cystinuria	12.9%
143	Multiple Epiphyseal Dysplasia	12.9%
144	Osteochondrodysplasias	12.9%
145	Friedreich Ataxia	12.7%
146	Wernicke Encephalopathy	12.6%
147	Optic Atrophy, Hereditary, Leber	12.2%
148	Necrobiosis Lipoidica Diabeticorum	12.1%
149	Kearns-Sayre syndrome	12%
150	Dwarfism	11.5%
151	Osteoarthropathy, Secondary Hypertrophic	11.5%
152	Xeroderma Pigmentosum	11.5%
153	Metal Metabolism, Inborn Errors	11.3%
154	Acidosis, Respiratory	11.3%
155	Adiposis Dolorosa	11.3%
156	Alkalosis, Respiratory	11.3%
157	Insulin Resistance	11.2%
158	Platybasia	11%
159	Variegate Porphyria	10.9%
160	Acute intermittent porphyria	10.9%
161	Porphyria Cutanea Tarda	10.9%
162	Kernicterus	10.9%
163	CREST Syndrome	10.7%
164	Hypercholesterolemia	10.6%
165	Hyperlipoproteinemias	10.6%
166	Hypertriglyceridemia	10.6%
167	Osteochondritis	10.1%
168	Gestational Diabetes	10%
169	Latent Autoimmune Diabetes in Adults	10%
170	Bone Diseases, Developmental	10%
171	Hyperostosis	10%
172	Osteitis	10%
173	Osteitis Deformans	10%
174	Osteochondrosis	10%
175	Spinal Diseases	10%
176	Congenital Hypothyroidism	10%
177	Diabetes Mellitus, Experimental	10%
178	Osteogenesis Imperfecta	10%
179	Gigantism	9.9%
180	Spinal Neoplasms	9.9%
181	Spondylitis	9.9%
182	Cerebral Amyloid Angiopathy	9.7%
183	Child Nutrition Disorders	9.4%
184	Hypervitaminosis A	9.4%
185	Infant Nutrition Disorders	9.4%
186	Malnutrition	9.4%
187	Pectus carinatum	9.1%
188	Nail-Patella Syndrome	9%
189	Marfan Syndrome	8.9%
190	Bone Diseases, Endocrine	8.8%
191	Primary amyloidosis	8.8%
192	Pectus excavatum	8.7%
193	Bone Diseases, Infectious	8.7%
194	Bone neoplasms	8.7%
195	Bone Resorption	8.6%
196	Aseptic Necrosis of Bone	8.6%
197	Rubinstein-Taybi Syndrome	8.2%
198	Amyotrophic Lateral Sclerosis	7.9%
199	Arthrogryposis	7.9%
200	Muscular Dystrophy	7.9%
201	Muscular Dystrophy, Duchenne	7.7%
202	Aicardi's syndrome	7.6%
203	Cystic Fibrosis	7.6%
204	Prader-Willi Syndrome	7.6%
205	CHARGE Syndrome	7.5%
206	Klippel-Feil Syndrome	7.5%
207	Synostosis	7.5%
208	Neoplastic Syndromes, Hereditary	7.4%
209	Discitis	7.3%
210	Pelger-Huet Anomaly	7.1%
211	Myasthenic Syndromes, Congenital	7.1%
212	Frontotemporal dementia	7%
213	Myotonic Dystrophy	6.8%
214	Acrocephalosyndactylia	6.8%
215	Ainhum	6.6%
216	Dysostoses	6.6%
217	Spinal Stenosis	6.6%
218	Spondylosis	6.6%
219	Intervertebral Disc Degeneration	6.6%
220	Anemia, Sickle Cell	6.6%
221	Thalassemia	6.6%
222	Fragile X Syndrome	6.5%
223	Tuberculosis, Spinal	6.5%
224	Craniosynostosis	6.4%
225	Syndactyly	6.4%
226	Brachycephaly	6.4%
227	Osteoarthritis, Spine	6.4%
228	Basal Cell Nevus Syndrome	6.3%
229	Holoprosencephaly	6.3%
230	Beckwith-Wiedemann Syndrome	6.2%
231	Wolf-Hirschhorn Syndrome	6.2%
232	Craniofacial Dysostosis	6.1%
233	Deficiency Diseases	6%
234	Starvation	6%
235	Refeeding Syndrome	6%
236	Eosinophilic Granuloma	5.9%
237	Alstrom Syndrome	5.8%
238	Contracture	5.8%
239	Fasciitis, Plantar	5.8%
240	Fasciitis	5.7%
241	Foot Deformities	5.7%
242	Arthropathy	5.7%
243	Kartagener Syndrome	5.7%
244	Osteomyelitis	5.7%
245	Periostitis	5.7%
246	Alveolar Bone Loss	5.6%
247	Femur Head Necrosis	5.6%
248	Osteolysis	5.6%
249	Autoimmune Lymphoproliferative Syndrome	5.6%
250	Smith-Magenis syndrome	5.6%
251	Cri-du-Chat Syndrome	5.5%
252	Down Syndrome	5.5%
253	Angioedemas, Hereditary	5.5%
254	Trisomy 21	5.5%
255	Ankylosing spondylitis	5.4%
256	Wiskott-Aldrich Syndrome	5.4%
257	Deformity	5.1%
258	Poland Syndrome	5.1%
259	Fibromyalgia	5%
260	Polymyalgia Rheumatica	5%
261	Metatarsalgia	5%
262	Jaw Diseases	5%
263	Ectodermal Dysplasia	5%
264	Aplasia Cutis Congenita	5%
265	Familial Mediterranean Fever	4.9%
266	Kallmann Syndrome	4.9%
267	Acromegaly	4.9%
268	Joint Tuberculosis	4.9%
269	Tuberculosis, Osteoarticular	4.9%
270	Bone Tuberculosis	4.9%
271	Chondrodysplasia Punctata	4.9%
272	Enchondromatosis	4.9%
273	Lordosis	4.9%
274	Osteosclerosis	4.9%
275	Spondylolysis	4.9%
276	kyphosis	4.9%
277	Kashin-Beck Disease	4.9%
278	Welander Distal Myopathy	4.9%
279	Cartilage Diseases	4.9%
280	Foot Diseases	4.9%
281	Myopathy	4.9%
282	Rheumatism	4.9%
283	Chondromalacia	4.9%
284	Spondylarthropathies	4.9%
285	Rett Syndrome	4.9%
286	Arthritis, Psoriatic	4.8%
287	Myotonia Congenita	4.8%
288	Tuberous Sclerosis	4.7%
289	Arthritis, Reactive	4.4%
290	Fetal Diseases	4.4%
291	Ischemic contracture	4.4%
292	Temporomandibular Joint Disorders	4.4%
293	Polycystic Kidney Diseases	4.4%
294	Kwashiorkor	4.4%
295	Magnesium Deficiency	4.4%
296	Potassium Deficiency	4.4%
297	Protein Deficiency	4.4%
298	Williams Syndrome	4.4%
299	Avitaminosis	4.4%
300	Mandibulofacial Dysostosis	4.3%
301	Sickle Cell Trait	4.3%
302	Limb Deformities, Congenital	4.3%
303	Craniofacial Abnormalities	4.3%
304	Talipes	4.3%
305	Goldenhar Syndrome	4.3%
306	Primary Ciliary Dyskinesia	4.2%
307	Rheumatic Fever	4.1%
308	Melorheostosis	4.1%
309	Osteopetrosis	4.1%
310	Spondylolisthesis	4.1%
311	Retinal Dysplasia	4.1%
312	Temporomandibular Joint Dysfunction Syndrome	4%
313	Aniridia	4%
314	Obesity	4%
315	Epidermolysis Bullosa	4%
316	Hip Contracture	3.8%
317	Periarthritis	3.8%
318	Jaw Abnormalities	3.8%
319	Cutis Laxa	3.7%
320	Retinitis Pigmentosa	3.7%
321	Gastroschisis	3.7%
322	Pigmentary retinopathy	3.7%
323	Rheumatoid Arthritis	3.7%
324	Juvenile arthritis	3.7%
325	Porokeratosis	3.7%
326	Keratoderma, Palmoplantar	3.7%
327	Chronic granulomatous disease	3.7%
328	Mastoiditis	3.7%
329	Petrositis	3.7%
330	Acute Chest Syndrome	3.6%
331	Ascorbic Acid Deficiency	3.5%
332	Vitamin A Deficiency	3.5%
333	Vitamin D Deficiency	3.5%
334	Vitamin E Deficiency	3.5%
335	Marasmus	3.5%
336	Palatal Neoplasms	3.4%
337	Meconium Aspiration Syndrome	3.4%
338	Congenital clubfoot	3.4%
339	Vertical Talus	3.4%
340	Duane Retraction Syndrome	3.4%
341	Arthritis	3.3%
342	Bursitis	3.3%
343	Joint Instability	3.3%
344	Myofascial Pain Syndromes	3.3%
345	Rhabdomyolysis	3.3%
346	Synovitis	3.3%
347	Joint laxity	3.3%
348	Polyarthritis	3.3%
349	Frozen shoulder	3.3%
350	Patellofemoral Pain Syndrome	3.3%
351	Prognathism	3.3%
352	Pseudoxanthoma Elasticum	3.3%
353	Maxillofacial Abnormalities	3.3%
354	Peutz-Jeghers Syndrome	3.3%
355	Thrombasthenia	3.3%
356	Antithrombin III Deficiency	3.3%
357	Protein C Deficiency	3.3%
358	Osteoarthritis, Knee	3.3%
359	Afibrinogenemia	3.3%
360	Dystonia Musculorum Deformans	3.3%
361	Factor VII Deficiency	3.3%
362	Factor X Deficiency	3.3%
363	Factor XII Deficiency	3.3%
364	Hemophilia A	3.3%
365	Activated Protein C Resistance	3.3%
366	Factor II deficiency	3.3%
367	Factor VIII Deficiency	3.3%
368	Factor V deficiency	3.3%
369	Factor XI Deficiency	3.3%
370	Hypoprothrombinemias	3.3%
371	Lafora Disease	3.3%
372	Unverricht-Lundborg Syndrome	3.3%
373	Anemia, Diamond-Blackfan	3.3%
374	Obesity, Abdominal	3.2%
375	Folic Acid Deficiency	3.1%
376	Pellagra	3.1%
377	Thiamine Deficiency	3.1%
378	Vitamin B 12 Deficiency	3.1%
379	Vitamin B 6 Deficiency	3.1%
380	Pyridoxine Deficiency	3.1%
381	Multiple Endocrine Neoplasia	3%
382	Laryngomalacia	3%
383	Dermatitis, Atopic	3%
384	Xeroderma	3%
385	Mobius Syndrome	3%
386	Beriberi	2.9%
387	Polycystic Kidney, Autosomal Dominant	2.9%
388	Compartment syndromes	2.9%
389	Maxillary Diseases	2.9%
390	Tendinitis	2.9%
391	Tendinopathy	2.9%
392	Pediatric Obesity	2.9%
393	Rheumatoid Nodule	2.9%
394	Hemarthrosis	2.9%
395	Myositis	2.9%
396	Tietze's Syndrome	2.9%
397	Isaacs syndrome	2.9%
398	Myotonic Disorders	2.9%
399	Classical Lissencephalies and Subcortical Band Heterotopias	2.8%
400	Amelia	2.8%
401	Arachnodactyly	2.8%
402	Ectromelia	2.8%
403	Hemimelia	2.8%
404	Phocomelia	2.8%
405	Sirenomelia	2.8%
406	Polydactyly	2.8%
407	Brachydactyly	2.8%
408	Plagiocephaly	2.8%
409	Lower Extremity Deformities, Congenital	2.8%
410	Upper Extremity Deformities, Congenital	2.8%
411	Hyperkeratosis, Epidermolytic	2.8%
412	Abdominal Cramps	2.8%
413	Abnormalities, Drug-Induced	2.8%
414	Amniotic Band Syndrome	2.8%
415	Asphyxia Neonatorum	2.8%
416	Infant, Premature, Diseases	2.8%
417	Situs Inversus	2.8%
418	Infantile Colic	2.8%
419	Micrognathism	2.7%
420	Pierre Robin Syndrome	2.7%
421	Microcephaly	2.7%
422	Macrocephaly	2.7%
423	Behcet Syndrome	2.7%
424	Vitamin K Deficiency	2.7%
425	Cleft Palate	2.6%
426	Charcot-Marie-Tooth Disease	2.6%
427	Felty Syndrome	2.6%
428	Nose Neoplasms	2.5%
429	Medial Tibial Stress Syndrome	2.5%
430	Retrognathia	2.5%
431	Anemia, Pernicious	2.5%
432	Muscle Cramp	2.5%
433	Eosinophilia-Myalgia Syndrome	2.5%
434	Muscle Rigidity	2.5%
435	Muscle Spasticity	2.5%
436	Cogwheel Rigidity	2.5%
437	Nuchal Rigidity	2.5%
438	Huntington Disease	2.5%
439	Eye Abnormalities	2.5%
440	Cardiovascular Abnormalities	2.5%
441	Papillon-Lefevre Disease	2.4%
442	Noonan Syndrome	2.4%
443	Skin Abnormalities	2.4%
444	Lymphatic Abnormalities	2.4%
445	Congenital Microtia	2.4%
446	Anemia, Neonatal	2.4%
447	Persistent Fetal Circulation Syndrome	2.4%
448	Congenital diaphragmatic hernia	2.4%
449	Umbilical hernia	2.4%
450	Scurvy	2.3%
451	Rheumatoid Vasculitis	2.3%
452	Chronic Fatigue Syndrome	2.3%
453	Nephroblastoma	2.3%
454	Giant Cell Epulis	2.2%
455	Muscle Weakness	2.2%
456	Musculoskeletal Pain	2.2%
457	Arthralgia	2.2%
458	Bunion	2.2%
459	Fibrodysplasia Ossificans Progressiva	2.2%
460	Myoglobinuria	2.2%
461	Myositis Ossificans	2.2%
462	Tenosynovitis	2.2%
463	Polyarthralgia	2.2%
464	Sacroiliitis	2.2%
465	Bronchomalacia	2.2%
466	Tracheomalacia	2.2%
467	Porencephaly	2.2%
468	Urogenital Abnormalities	2.2%
469	Neonatal Abstinence Syndrome	2.1%
470	Adenomatous Polyposis Coli	2.1%
471	Sicca Syndrome	2.1%
472	Sjogren's Syndrome	2.1%
473	Fetal Growth Retardation	2.1%
474	Fetal Hypoxia	2.1%
475	Congenital nystagmus	2.1%
476	Fetal Alcohol Spectrum Disorders	2.1%
477	Toxoplasmosis, Congenital	2.1%
478	Hydrops Fetalis	2.1%
479	Anencephaly	2.1%
480	Syphilis, Congenital	2.1%
481	Klinefelter Syndrome	2%
482	Turner Syndrome	2%
483	Myalgia	2%
484	Multiple Endocrine Neoplasia Type 1	2%
485	Arthritis, Infectious	1.9%
486	Anterior Compartment Syndrome	1.9%
487	Enthesopathy	1.9%
488	Arthritis, Experimental	1.9%
489	Abdominal Compartment Syndrome	1.9%
490	Polymyositis	1.9%
491	Chorioamnionitis	1.8%
492	Dural Arteriovenous Fistula	1.8%
493	Dextrocardia	1.8%
494	Subacute Combined Degeneration	1.8%
495	Hip Dislocation	1.7%
496	Shoulder Dislocation	1.7%
497	Hip Dysplasia	1.7%
498	Orbital Myositis	1.7%
499	Dupuytren Contracture	1.7%
500	Abnormalities, Radiation-Induced	1.7%
501	Prune Belly Syndrome	1.6%
502	Twins, Conjoined	1.6%
503	Waardenburg Syndrome	1.6%
504	Pyomyositis	1.6%
505	Scimitar Syndrome	1.5%
506	Ophthalmia Neonatorum	1.5%
507	Shoulder Pain	1.4%
508	Anophthalmos	1.4%
509	Anus, Imperforate	1.4%
510	Hydranencephaly	1.4%
511	Microphthalmos	1.4%
512	Neural Tube Defects	1.4%
513	Paralysis, Obstetric	1.4%
514	Retinopathy of Prematurity	1.4%
515	Tethered Cord Syndrome	1.4%
516	Iniencephaly	1.4%
517	Craniorachischisis	1.4%
518	Exencephaly	1.4%
519	Septo-Optic Dysplasia	1.4%
520	Cortical Dysplasia	1.4%
521	Malformations of Cortical Development	1.4%
522	Anorectal Malformations	1.4%
523	Denys-Drash Syndrome	1.4%
524	Bronchopulmonary Dysplasia	1.4%
525	Blepharophimosis	1.3%
526	Laryngostenosis	1.3%
527	Mouth Abnormalities	1.3%
528	Respiratory Distress Syndrome, Newborn	1.3%
529	Esophageal Atresia	1.3%
530	Intestinal Atresia	1.3%
531	Horseshoe Kidney	1.3%
532	Acrodermatitis	1.2%
533	Lymphangiectasis, Intestinal	1.2%
534	Gianotti-Crosti Syndrome	1.2%
535	Choanal Atresia	1.1%
536	Tracheobronchomegaly	1.1%
537	Laryngocele	1.1%
538	Choledochal Cyst	1.1%
539	Hermaphroditism	1.1%
540	Disorders of Sex Development	1.1%
541	Cryptorchidism	1.1%
542	Hypospadias	1.1%
543	Dermatomyositis	1.1%
544	Central Nervous System Cysts	1.1%
545	Dandy-Walker Syndrome	1.1%
546	Leukomalacia, Periventricular	1.1%
547	POEMS Syndrome	1.1%
548	Bladder Exstrophy	1%
549	Epispadias	1%
550	Multicystic Dysplastic Kidney	1%
551	Ectopia Cordis	0.9%
552	Meningomyelocele	0.9%
553	Spina Bifida	0.9%
554	Single umbilical artery	0.9%
555	Aortic coarctation	0.8%
556	Cor Triatriatum	0.8%
557	Coronary Vessel Anomalies	0.8%
558	Dental Enamel Hypoplasia	0.8%
559	Patent ductus arteriosus	0.8%
560	Ebstein Anomaly	0.8%
561	Heart Septal Defects	0.8%
562	Hyaline Membrane Disease	0.8%
563	Hypodontia	0.8%
564	Macrostomia	0.8%
565	Meningocele	0.8%
566	Microstomia	0.8%
567	Tetralogy of Fallot	0.8%
568	Transposition of Great Vessels	0.8%
569	Hypoplastic Left Heart Syndrome	0.8%
570	May-Thurner Syndrome	0.8%
571	Encephalocele	0.8%
572	Wolff-Parkinson-White Syndrome	0.8%
573	Radicular Cyst	0.8%
574	Hyperandrogenism	0.7%
575	Long QT Syndrome	0.7%
576	Tricuspid Atresia	0.7%
577	Arrhythmogenic Right Ventricular Dysplasia	0.7%
578	Gonadal Dysgenesis	0.7%
579	Adrenogenital Syndrome	0.7%
580	Ovotesticular Disorders of Sex Development	0.7%
581	Dermal Sinus	0.7%
582	Spina Bifida Cystica	0.7%
583	Spina Bifida Occulta	0.7%
584	Lissencephaly	0.7%
585	Polymicrogyria	0.7%
586	Pachygyria	0.7%
587	Schizencephaly	0.7%
588	Periventricular Nodular Heterotopia	0.7%
589	Aortopulmonary Septal Defect	0.6%
590	Double Outlet Right Ventricle	0.6%
591	Endocardial Cushion Defects	0.6%
592	Myocardial bridging	0.6%
593	Aorticopulmonary Septal Defect	0.6%
594	Romano-Ward Syndrome	0.5%
595	Truncus Arteriosus, Persistent	0.5%
596	Arteriovenous fistula	0.4%

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