Table 4: List of Rare Diseases and Related Terms as per US ...

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1287 Cleft hand absent tibia 1288 Cleft lip and palate malrotation cardiopathy 1289 Cleft lip and/or palate with mucous cysts of lower 1290 Cleft lip palate dysmorphism Kumar type 1291 Cleft lip palate mental retardation corneal opacity 1292 Cleft lip palate oligodontia syndactyly pili torti 1293 Cleft lip palate pituitary deficiency 1294 Cleft lip palate-tetraphocomelia 1295 Cleft lower lip cleft lateral canthi chorioretinal 1296 Cleft palate cardiac defect ectrodactyly 1297 Cleft palate colobomata radial synostosis deafness 1298 Cleft palate heart disease polydactyly absent tibia 1299 Cleft palate lateral synechia syndrome 1300 Cleft palate short stature vertebral anomalies 1301 Cleft palate stapes fixation oligodontia 1302 Cleft palate X-linked 1303 Cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing loss 1304 Cleft tongue syndrome 1305 Cleft upper lip median cutaneous polyps 1306 Cleidocranial dysplasia 1307 Cleidocranial dysplasia recessive form 1308 Cleidorhizomelic syndrome 1309 C-like syndrome 1310 Cloacal exstrophy 1311 Clostridium difficile 1312 Clostridium sordellii 1313 CLOVES syndrome 1314 Cluster headache 1315 Cluttering 1316 CMV antenatal infection 1317 COACH syndrome 1318 Coal worker's pneumoconiosis 1319 Coarctation of aorta dominant 1320 Coarse face hypotonia constipation 1321 Coats disease 1322 Cocaine antenatal infection 1323 Coccidioidomycosis 1324 Coccygodynia
1325 Cochleosaccular degeneration of the inner ear and progressive cataracts 1326 Cockayne syndrome 1327 Cockayne syndrome type I 1328 Cockayne syndrome type II 1329 Cockayne syndrome type III 1330 CODAS syndrome 1331 Coenzyme Q cytochrome c reductase deficiency of 1332 Coenzyme Q10 deficiency 1333 Coffin syndrome 1 1334 Coffin-Lowry syndrome 1335 Coffin-Siris syndrome 1336 Cogan-Reese syndrome 1337 Cogan's syndrome 1338 Cohen Hayden syndrome 1339 Cohen Lockood Wyborney syndrome 1340 Cohen syndrome 1341 Cold agglutinin disease 1342 Cold contact urticaria 1343 Cole Carpenter syndrome 1344 Collagenopathy type 2 alpha 1 1345 Collagenous colitis 1346 Collagenous gastritis 1347 Collecting duct carcinoma 1348 Collins Pope syndrome 1349 Collins Sakati syndrome 1350 Colloid cysts of third ventricle 1351 Coloboma chorioretinal cerebellar vermis aplasia 1352 Coloboma of alar-nasal cartilages with telecanthus 1353 Coloboma of eye lens 1354 Coloboma of iris 1355 Coloboma of macula 1356 Coloboma of macula with type B brachydactyly 1357 Coloboma of optic nerve 1358 Coloboma of optic papilla 1359 Coloboma porencephaly hydronephrosis 1360 Coloboma, cleft lip/palate and mental retardation syndrome 1361 Colobomata unilobar lung heart defect 1362 Colobomatous microphthalmia heart disease hearing 1363 Colonic atresia
Page 1 and 2: Table 4: List of Rare Diseases and
Page 3 and 4: 77 Acrodysplasia with ossification
Page 5 and 6: 156 Adenosine deaminase deficiency
Page 7 and 8: 235 Alopecia mental retardation syn
Page 9 and 10: 313 Anal sphincter dysplasia 314 An
Page 11 and 12: 389 Anterior segment mesenchymal dy
Page 13 and 14: 467 Arthrogryposis renal dysfunctio
Page 15 and 16: 542 Autosomal recessive neuronal ce
Page 17 and 18: 621 Becker muscular dystrophy 622 B
Page 19 and 20: 699 Blastoma 700 Blastomycosis 701
Page 21 and 22: 777 Braddock Jones Superneau syndro
Page 23 and 24: 857 Camurati-Engelmann disease 858
Page 25 and 26: 937 Cataract, autosomal recessive c
Page 27 and 28: 1012 Ceroid lipofuscinosis neuronal
Page 29 and 30: 1090 Chitayat Meunier Hodgkinson sy
Page 31 and 32: 1170 Chromosome 16p deletion 1171 C
Page 33: 1249 Chronic atypical neutrophilic
Page 37 and 38: 1404 Congenital aplastic anemia 140
Page 39 and 40: 1482 Congenital nonprogressive myop
Page 41 and 42: 1561 Cranioacrofacial syndrome 1562
Page 43 and 44: 1641 Cutis laxa, autosomal recessiv
Page 45 and 46: 1713 Deafness, autosomal dominant n
Page 47 and 48: 1790 Diamond-Blackfan anemia 2 1791
Page 49 and 50: 1868 Duane syndrome 1869 Duane synd
Page 51 and 52: 1946 EAF 1947 Eagle syndrome 1948 E
Page 53 and 54: 2024 Endocardial fibroelastosis 202
Page 55 and 56: 2102 Erythropoietic uroporphyria as
Page 57 and 58: 2181 Familial exudative vitreoretin
Page 59 and 60: 2260 Fetal brain disruption sequenc
Page 61 and 62: 2338 Frank Ter Haar syndrome 2339 F
Page 63 and 64: 2418 Gay Feinmesser Cohen syndrome
Page 65 and 66: 2497 Glucocorticoid resistance 2498
Page 67 and 68: 2577 Gray platelet syndrome 2578 Gr
Page 69 and 70: 2656 Hemicrania continua 2657 Hemif
Page 71 and 72: 2734 Hereditary nodular heterotopia
Page 73 and 74: 2814 Horner's syndrome 2815 Horsesh
Page 75 and 76: 2894 Hyperlipoproteinemia type 4 28
Page 77 and 78: 2970 Hypopituitarism postaxial poly
Page 79 and 80: 3045 Immune dysfunction with T-cell
Page 81 and 82: 3121 Intravascular papillary endoth
Page 83 and 84: 3201 Juvenile Scleroderma 3202 Juve
Page 85 and 86:
3281 Kohlschutter Tonz syndrome 328
Page 87 and 88:
3360 Lattice corneal dystrophy type
Page 89 and 90:
hypogammaglobulinema 3439 Leukoence
Page 91 and 92:
3517 Long QT syndrome 10 3518 Long
Page 93 and 94:
3594 Mal de debarquement 3595 Malak
Page 95 and 96:
3672 Maturity-onset diabetes of the
Page 97 and 98:
3750 Mental retardation arachnodact
Page 99 and 100:
3824 Methylmalonic acidemia with ho
Page 101 and 102:
3901 Mikulicz disease 3902 Miles-Ca
Page 103 and 104:
3977 Muckle-Wells syndrome 3978 Muc
Page 105 and 106:
4055 Myasthenia gravis 4056 Myasthe
Page 107 and 108:
4134 Nance-Horan syndrome 4135 Narc
Page 109 and 110:
4213 Neuromyelitis optica spectrum
Page 111 and 112:
4293 Nystagmus, hereditary vertical
Page 113 and 114:
4372 Optic atrophy 2 4373 Optic atr
Page 115 and 116:
4451 Osteopetrosis autosomal domina
Page 117 and 118:
4531 Papular urticaria 4532 Paracoc
Page 119 and 120:
4611 Pentosuria 4612 Penttinen-Aula
Page 121 and 122:
4688 Pilotto syndrome 4689 Pineal p
Page 123 and 124:
4766 Pontocerebellar hypoplasia typ
Page 125 and 126:
4844 Primary pigmented nodular adre
Page 127 and 128:
4923 Pseudopelade of Brocq 4924 Pse
Page 129 and 130:
5003 Radiation induced cancer 5004
Page 131 and 132:
5079 Restless legs syndrome, suscep
Page 133 and 134:
5157 Rhizomelic syndrome 5158 RHYNS
Page 135 and 136:
5237 Sacral defect with anterior me
Page 137 and 138:
5317 Seckel syndrome 5318 Secretory
Page 139 and 140:
5391 Short stature, cranial hyperos
Page 141 and 142:
5470 Spastic ataxia Charlevoix-Sagu
Page 143 and 144:
5549 Spinocerebellar ataxia 27 5550
Page 145 and 146:
5625 Spondylometaphyseal dysplasia
Page 147 and 148:
5704 Superior limbic keratoconjunct
Page 149 and 150:
5781 T-cell immunodeficiency, conge
Page 151 and 152:
5859 Thyroid cancer, childhood 5860
Page 153 and 154:
5939 Trichomalacia 5940 Trichomegal
Page 155 and 156:
6017 Ulcerative proctitis 6018 Uler
Page 157 and 158:
6096 Verloove Vanhorick Brubakk syn
Page 159 and 160:
6176 Weyers acrofacial dysostosis 6
Page 161 and 162:
6253 X-linked mental retardation Gu
Page 163:
Note: 6333 4-hydroxyphenylacetic ac
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Table 4: List of Rare Diseases and Related Terms as per US ...

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