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

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2299 Finger locking recurrent with intrauterine growth retardation and proportionate short stature 2300 Fish-eye disease 2301 Fitz-Hugh-Curtis syndrome 2302 Fitzsimmons syndrome 2303 Fitzsimmons Walson Mellor syndrome 2304 Fitzsimmons-Guilbert syndrome 2305 Flat umbilicus familial 2306 Flavimonas oryzihabitans 2307 Floating-Harbor syndrome 2308 Florid cemento-osseous dysplasia 2309 Florid cystic endosalpingiosis of the uterus 2310 Florid papillomatosis of the nipple 2311 FLOTCH syndrome 2312 Flynn Aird syndrome 2313 Focal alopecia congenital megalencephaly 2314 Focal cortical dysplasia of Taylor 2315 Focal dermal hypoplasia 2316 Focal dystonia 2317 Focal facial dermal dysplasia 2318 Focal or multifocal malformations in neuronal migration 2319 Foix Chavany Marie syndrome 2320 Follicle-stimulating hormone deficiency, isolated 2321 Follicular dendritic cell tumor 2322 Follicular lymphoma 2323 Follicular lymphoreticuloma 2324 Fontaine Farriaux Blanckaert syndrome 2325 Forbes Albright syndrome 2326 Formaldehyde poisoning 2327 Fountain syndrome 2328 Fournier gangrene 2329 Fowler's syndrome 2330 Fox-Fordyce disease 2331 Fragile X syndrome 2332 Fragile X syndrome type 1 2333 Fragile X syndrome type 2 2334 Fragile X syndrome type 3 2335 Fragile XE syndrome 2336 Franceschini Vardeu Guala syndrome 2337 Franek Bocker kahlen syndrome
2338 Frank Ter Haar syndrome 2339 Fraser Jequier Chen syndrome 2340 Fraser like syndrome 2341 Fraser syndrome 2342 Frasier syndrome 2343 FRAXD 2344 Free sialic acid storage disease 2345 Freeman Sheldon syndrome 2346 Freiberg's disease 2347 Freire-Maia odontotrichomelic syndrome 2348 Frenkel Russe syndrome 2349 Frey's syndrome 2350 Frias syndrome 2351 Friedel Heid Grosshans syndrome 2352 Friedman Goodman syndrome 2353 Friedreich ataxia 2354 Friedreich ataxia congenital glaucoma 2355 Frints De Smet Fabry Fryns syndrome 2356 Froelich syndrome 2357 Frontal fibrosing alopecia 2358 Fronto nasal malformation cloacal exstrophy 2359 Frontofacionasal dysplasia 2360 Frontometaphyseal dysplasia 2361 Frontonasal dysplasia 2362 Frontonasal dysplasia acromelic 2363 Frontonasal dysplasia Klippel Feil syndrome 2364 Frontonasal dysplasia phocomelic upper limbs 2365 Frontotemporal dementia 2366 Frontotemporal dementia, ubiquitin-positive 2367 Froster-Huch syndrome 2368 Fructose-1,6-bisphosphatase deficiency 2369 Fryns Fabry Remans syndrome 2370 Fryns Hofkens Fabry syndrome 2371 Fryns smeets thiry syndrome 2372 Fryns syndrome 2373 Fuchs atrophia gyrata chorioideae et retinae 2374 Fuchs heterochromic iridocyclitis 2375 Fucosidosis 2376 Fucosidosis type 1 2377 Fuhrmann syndrome
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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 and 34: 1249 Chronic atypical neutrophilic
Page 35 and 36: 1325 Cochleosaccular degeneration o
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: 2260 Fetal brain disruption sequenc
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
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4451 Osteopetrosis autosomal domina
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4531 Papular urticaria 4532 Paracoc
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4611 Pentosuria 4612 Penttinen-Aula
Page 121 and 122:
4688 Pilotto syndrome 4689 Pineal p
Page 123 and 124:
4766 Pontocerebellar hypoplasia typ
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4844 Primary pigmented nodular adre
Page 127 and 128:
4923 Pseudopelade of Brocq 4924 Pse
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5003 Radiation induced cancer 5004
Page 131 and 132:
5079 Restless legs syndrome, suscep
Page 133 and 134:
5157 Rhizomelic syndrome 5158 RHYNS
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5237 Sacral defect with anterior me
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5317 Seckel syndrome 5318 Secretory
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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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