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

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2774 Hirschsprung disease type d brachydactyly 2775 Hirschsprung microcephaly cleft palate 2776 Hirschsprung nail hypoplasia dysmorphism 2777 Hirschsprung's disease 2778 Hirsutism skeletal dysplasia mental retardation 2779 His bundle tachycardia 2780 Histidinemia 2781 Histidinuria renal tubular defect 2782 Histiocytosis with joint contractures and sensorineural deafness 2783 Histiocytosis, Non-Langerhans-Cell 2784 Hittner Hirsch Kreh syndrome 2785 Hm syndrome 2786 HMG CoA lyase deficiency 2787 HMG CoA synthetase deficiency 2788 Ho Kaufman Mcalister syndrome 2789 Hodgkin disease, X-linked pseudoautosomal 2790 Hodgkin lymphoma 2791 Hodgkin lymphoma, childhood 2792 Hodgkin lymphoma, during pregnancy 2793 Holmes Borden syndrome 2794 Holoacardius amorphus 2795 Holocarboxylase synthetase deficiency 2796 Holoprosencephaly 2797 Holoprosencephaly caudal dysgenesis 2798 Holoprosencephaly ectrodactyly cleft lip palate 2799 Holoprosencephaly, recurrent infections, and monocytosis 2800 Holt-Oram syndrome 2801 Holzgreve syndrome 2802 Homocarnosinosis 2803 Homocysteinemia 2804 Homocysteinemia due to MTHFR deficiency 2805 Homocystinuria 2806 Homocystinuria due to CBS deficiency 2807 Homocystinuria due to defect in methylation cbl e 2808 Homocystinuria due to defect in methylation cbl g 2809 Homologous wasting disease 2810 Hooft disease 2811 Hoon Hall syndrome 2812 Hordnes Engebretsen Knudtson syndrome 2813 Horn Kolb syndrome
2814 Horner's syndrome 2815 Horseshoe kidney 2816 Houlston Ironton Temple syndrome 2817 Hoyeraal Hreidarsson syndrome 2818 HTLV-1 associated myelopathy/tropical spastic paraparesis 2819 Human granulocytic ehrlichiosis 2820 Human monocytic ehrlichiosis 2821 Human spumaretrovirus infection 2822 Human T-cell leukemia virus type 1 2823 Human T-cell leukemia virus type 2 2824 Human T-cell leukemia virus type 3 2825 Humeroradial synostosis 2826 Humeroradioulnar synostosis 2827 Hunter Carpenter Macdonald syndrome 2828 Hunter Macpherson syndrome 2829 Hunter Mcdonald syndrome 2830 Hunter Rudd Hoffmann syndrome 2831 Hunter-McAlpine syndrome 2832 Huntington disease 2833 Hurst Hallam Hockey syndrome 2834 Hurthle cell thyroid cancer 2835 Hutchinson incisors 2836 Hutterite cerebroosteonephrodysplasia syndrome 2837 Hyalinosis systemic short stature 2838 Hydatidiform mole 2839 Hydatidosis 2840 Hyde Forster Mccarthy Berry syndrome 2841 Hydranencephaly 2842 Hydroa vacciniforme 2843 Hydroa vacciniforme, familial 2844 Hydrocephalus 2845 Hydrocephalus autosomal recessive 2846 Hydrocephalus craniosynostosis bifid nose 2847 Hydrocephalus due to congenital stenosis of aqueduct of sylvius 2848 Hydrocephalus growth retardation skeletal anomalies 2849 Hydrocephalus obesity hypogonadism 2850 Hydrocephalus skeletal anomalies 2851 Hydrocephalus, costovertebral dysplasia, and Sprengel anomaly 2852 Hydrocephaly corpus callosum agenesis diaphragmatic hernia 2853 Hydrolethalus 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 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: 2734 Hereditary nodular heterotopia
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
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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
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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