Disease Name Symbol Acronym
Haemonchiasis HMN005
Haemophilus Influenzae HMP009
Haemophilus Meningitis HMP030
Haim-Munk Syndrome HMM002 HMS
Hair Disease HRD018
Hair Follicle Neoplasm HRF001
Hair Morphology 1 HRM022 HRM1
Hair Morphology 2 HRM021 HRM2
Hairy Cell Leukemia HRY003 HCL
Hairy Ears, Y-Linked HRY009
Hairy Elbows HRY005
Hairy Tongue HRY002
Hajdu-Cheney Syndrome HJD001 HJCYS
Hallermann-Streiff Syndrome HLL001 HSS
Hallucinogen Abuse HLL002
Hallucinogen Dependence HLL005
Halothane Hepatitis HLT002
Halperin-Birk Syndrome HLP033 HLBKS
Hamamy Syndrome HMM004 HMMS
Hand Skill, Relative HND015 HSR
Hand, Foot and Mouth Disease HND002
Hand-Foot-Genital Syndrome HND004 HFG
Hantavirus Hemorrhagic Fever with Renal Syndrome HNT019 HFRS
Hantavirus Pulmonary Syndrome HNT002 HPS
Hao-Fountain Syndrome HFN001 HAFOUS
Hard Palate Cancer HRD005
Harderoporphyria HRD090 HARPO
Hardikar Syndrome HRD037 HDKR
Harel-Yoon Syndrome HRL006 HAYOS
Hartnup Disorder HRT031 HND
Hartsfield Syndrome HRT030 HRTFDS
Hashimoto Encephalopathy HSH004 SREAT
Hashimoto Thyroiditis HSH003 HT
Haverhill Fever HVR001
Hawkinsinuria HWK001 HWKS
Head and Neck Cancer HDN003 HNC
Headache HDC001
Hearing Loss, Cisplatin-Induced HRN018 CIHL
Hearing Loss, Noise-Induced HRN029 NIHL
Heart and Brain Malformation Syndrome HRT037 HBMS
Heart Aneurysm HRT006
Heart Block, Congenital HRT035
Heart Cancer HRT007
Heart Conduction Disease HRT008
Heart Defects, Congenital, and Other Congenital Anomalies HRT039 HDCA
Heart Disease HRT032
Heart Fibrosarcoma HRT002
Heart Leiomyosarcoma HRT005
Heart Lymphoma HRT003
Heart Sarcoma HRT010
Heart Septal Defect HRT011
Heart Tumor HRT017
Heart Valve Disease HRT012
Heart, Malformation of HRT038
Heart-Hand Syndrome, Slovenian Type HRT018 HHS-SLOVENIAN
Heat-Shock Rna 1 HTS002 HSR1
Heavy Chain Disease HVY001 HCD
Heel Spur HLS001
Heimler Syndrome 1 HML047 HMLR1
Heimler Syndrome 2 HML046 HMLR2
Heinz Body Anemias HNZ004 HEIBAN
Helicobacter Pylori Infection HLC007
Helix Syndrome HLX001 HELIX
Hellp Syndrome HLL004
Helsmoortel-Van Der Aa Syndrome HLS003 HVDAS
Hemangioblastoma HMN009
Hemangioendothelioma HMN016
Hemangioma HMN010
Hemangioma of Intra-Abdominal Structure HMN011
Hemangioma of Liver HMN004
Hemangioma of Lung HMN012
Hemangioma of Spleen HMN003
Hemangioma of Subcutaneous Tissue HMN008
Hemangioma, Capillary Infantile HMN027 HCI
Hemangioma-Thrombocytopenia Syndrome HMN035 KMP
Hemangiopericytoma, Malignant HMN036
Hemarthrosis HMR002
Hematocele of Tunica Vaginalis Testis HMT001
Hematocrit/hemoglobin Quantitative Trait Locus 1 HMT005 HCHGQ1
Hematocrit/hemoglobin Quantitative Trait Locus 2 HMT006 HCHGQ2
Hematocrit/hemoglobin Quantitative Trait Locus 3 HMT007 HCHGQ3
Hematologic Cancer HMT002
Hematuria, Benign Familial HMT008 BFH
Heme Oxygenase 1 Deficiency HMX003 HMOX1D
Hemidystonia HMD003
Hemifacial Hyperplasia HMF009
Hemifacial Spasm HMF004
Hemihyperplasia, Isolated HMH004 IH
Hemihyperplasia-Multiple Lipomatosis Syndrome HMH003 HHML
Hemimegalencephaly HMM003
Hemimelia HMM005
Hemiplegia HMP005
Hemochromatosis Type 2 HMC009 JHH
Hemochromatosis, Neonatal HMC038 NH
Hemochromatosis, Type 1 HMC039 HFE1
Hemochromatosis, Type 2a HMC021 HFE2A
Hemochromatosis, Type 2b HMC019 HFE2B
Hemochromatosis, Type 3 HMC010 HFE3
Hemochromatosis, Type 4 HMC035 HFE4
Hemochromatosis, Type 5 HMC034 HFE5
Hemoglobin C Disease HMG001
Hemoglobin C-Beta-Thalassemia Syndrome HMG027
Hemoglobin D Disease HMG004
Hemoglobin E Disease HMG003
Hemoglobin E-Beta-Thalassemia Syndrome HMG026
Hemoglobin H Disease HMG032 HBH
Hemoglobin Lepore-Beta-Thalassemia Syndrome HMG028
Hemoglobin Se Disease HMG029
Hemoglobin, High Altitude Adaptation HMG031 HALAH
Hemoglobinopathy HMG005
Hemoglobinopathy Toms River HMG024
Hemoglobinuria HMG002
Hemolytic Anemia HML002
Hemolytic Anemia Due to Erythrocyte Adenosine Deaminase Overproduction HML041
Hemolytic Anemia Due to Glutathione Reductase Deficiency HML010 HAGRD
Hemolytic Anemia, Cd59-Mediated, with or Without Immune-Mediated Polyneuropathy HML042 HACD59
Hemolytic Anemia, Congenital, X-Linked HML053 HACXL
Hemolytic Anemia, Nonspherocytic, Due to Glucose Phosphate Isomerase Deficiency HML021 HA-GPID
Hemolytic Anemia, Nonspherocytic, Due to Hexokinase Deficiency HML052 HK DEFICIENCY
Hemolytic Disease of Fetus and Newborn, Rh-Induced HML058 HDFNRH
Hemolytic Uremic Syndrome, Atypical 1 HML033 AHUS1
Hemolytic Uremic Syndrome, Atypical 2 HML035 AHUS2
Hemolytic Uremic Syndrome, Atypical 3 HML034 AHUS3
Hemolytic Uremic Syndrome, Atypical 4 HML032 AHUS4
Hemolytic Uremic Syndrome, Atypical 5 HML037 AHUS5
Hemolytic Uremic Syndrome, Atypical 6 HML036 AHUS6
Hemolytic-Uremic Syndrome HML001 HUS
Hemometra HMM001
Hemopericardium HMP001
Hemophagocytic Lymphohistiocytosis HMP002
Hemophagocytic Lymphohistiocytosis, Familial, 1 HMP022 FHL1
Hemophagocytic Lymphohistiocytosis, Familial, 2 HMP012 FHL2
Hemophagocytic Lymphohistiocytosis, Familial, 3 HMP013 FHL3
Hemophagocytic Lymphohistiocytosis, Familial, 4 HMP014 FHL4
Hemophagocytic Lymphohistiocytosis, Familial, 5, with or Without Microvillus Inclusion Disease HMP033 FHL5
Hemophilia HMP007
Hemophilia a HMP029 HEMA
Hemophilia B HMP004 HEMB
Hemophilia B Leyden HMP034
Hemopneumothorax HMP003
Hemorrhage, Intracerebral HMR039 ICH
Hemorrhagic Cystitis HMR023
Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Cataracts HMR018 HDBSCC
Hemorrhagic Disease HMR003
Hemorrhagic Disease Due to Alpha-1-Antitrypsin Pittsburgh Mutation HMR041
Hemorrhoid HMR005 PILES
Hemosiderosis HMS001
Hengel-Maroofian-Schols Syndrome HNG004 HEMARS
Hennekam Lymphangiectasia-Lymphedema Syndrome 1 HNN005 HKLLS1
Hennekam Lymphangiectasia-Lymphedema Syndrome 2 HNN004 HKLLS2
Hennekam Lymphangiectasia-Lymphedema Syndrome 3 HNN006 HKLLS3
Hennekam Syndrome HNN001
Henoch-Schoenlein Purpura HNC001 HSP -
Heparin Cofactor Ii Deficiency HPR006 THPH10
Heparin-Induced Thrombocytopenia HPR003 HAT
Hepatic Adenomas, Familial HPT082 HEPAF
Hepatic Angiomyolipoma HPT006
Hepatic Coma HPT004
Hepatic Encephalopathy HPT019
Hepatic Fibrosis, Severe Due to Schistosoma Mansoni Infection HPT084 SM2
Hepatic Flexure Cancer HPT005
Hepatic Infarction HPT081
Hepatic Lipase Deficiency HPT025 HL DEFICIENCY
Hepatic Osteogenic Sarcoma HPT017
Hepatic Tuberculosis HPT008
Hepatic Vascular Disease HPT020
Hepatic Veno-Occlusive Disease HPT046
Hepatic Venoocclusive Disease with Immunodeficiency HPT077 VODI
Hepatitis HPT021
Hepatitis a HPT003
Hepatitis B HPT016 HBV
Hepatitis C HPT001 NANBH
Hepatitis C Virus HPT073 HCV
Hepatitis D HPT015 HDV
Hepatitis E HPT007
Hepatitis, Fulminant Viral HPT085 FVH
Hepatoblastoma HPT022
Hepatocellular Adenoma HPT067
Hepatocellular Carcinoma HPT023 HCC
Hepatocellular Clear Cell Carcinoma HPT011
Hepatoid Adenocarcinoma HPT079
Hepatopulmonary Syndrome HPT009
Hepatorenal Syndrome HPT014
Hepatorenocardiac Degenerative Fibrosis HPT087 HRCDF
Hepatosplenic T-Cell Lymphoma HPT070
Her2-Receptor Negative Breast Cancer HR2002
Her2-Receptor Positive Breast Cancer HR2001
Hereditary Alpha Tryptasemia Syndrome HRD193
Hereditary Amyloidosis HRD039
Hereditary Angioedema HRD002 HAE
Hereditary Angioedema with C1inh Deficiency HRD208
Hereditary Angioedema with Normal C1inh Not Related to F12 or Plg Variant HRD225
Hereditary Ataxia HRD026 SCA
Hereditary Breast Cancer HRD117
Hereditary Breast Ovarian Cancer Syndrome HRD200
Hereditary Central Diabetes Insipidus HRD156
Hereditary Cerebral Amyloid Angiopathy HRD084
Hereditary Choroidal Atrophy HRD019
Hereditary Combined Deficiency of Vitamin K-Dependent Clotting Factors HRD160 VKCFD
Hereditary Continuous Muscle Fiber Activity HRD222
Hereditary Conventional Renal Cell Carcinoma HRD003
Hereditary Distal Renal Tubular Acidosis HRD219
Hereditary Dystonia HRD198
Hereditary Elliptocytosis HRD012 HE
Hereditary Episodic Ataxia HRD212
Hereditary Hearing Loss and Deafness HRD199
Hereditary Hemorrhagic Telangiectasia HRD008 HHT
Hereditary Hypercarotenemia and Vitamin a Deficiency HRD143
Hereditary Late-Onset Parkinson Disease HRD173 LOPD
Hereditary Leiomyomatosis and Renal Cell Cancer HRD029 HLRCC
Hereditary Lymphedema HRD007
Hereditary Lymphedema I HRD202 PCL
Hereditary Lymphedema Ia HRD204
Hereditary Lymphedema Ic HRD100
Hereditary Lymphedema Id HRD203
Hereditary Lymphedema Ii HRD206 LMPH2
Hereditary Melanoma HRD223
Hereditary Mixed Polyposis Syndrome HRD144 HMPS
Hereditary Motor and Sensory Neuropathy V HRD138 HMSN5
Hereditary Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum HRD103 ACCPN
Hereditary Motor and Sensory Neuropathy, Type Iic HRD094 HMSN2C
Hereditary Multiple Exostoses HRD001
Hereditary Multiple Osteochondromas HRD104
Hereditary Nephrogenic Diabetes Insipidus HRD221
Hereditary Neuroendocrine Tumor of Small Intestine HRD181
Hereditary Neuropathies HRD088
Hereditary Optic Neuropathy HRD217
Hereditary Palmoplantar Keratoderma HRD216
Hereditary Paraganglioma-Pheochromocytoma Syndromes HRD031 FPGL
Hereditary Periodic Fever Syndrome HRD214
Hereditary Persistence of Fetal Hemoglobin-Beta-Thalassemia Syndrome HRD183
Hereditary Persistence of Fetal Hemoglobin-Intellectual Disability Syndrome HRD228
Hereditary Persistence of Fetal Hemoglobin-Sickle Cell Disease Syndrome HRD180
Hereditary Poikiloderma HRD213
Hereditary Pulmonary Alveolar Proteinosis HRD171
Hereditary Renal Cell Carcinoma HRD020
Hereditary Retinal Dystrophy HRD016
Hereditary Sensorimotor Neuropathy with Hyperelastic Skin HRD105
Hereditary Sensory and Autonomic Neuropathy Type 1 HRD201 HSAN1
Hereditary Sensory Neuropathy HRD021 HSAN
Hereditary Site-Specific Ovarian Cancer Syndrome HRD114
Hereditary Spastic Paraplegia HRD010 FSP
Hereditary Spastic Paraplegia 23 HRD210 SPG23
Hereditary Spastic Paraplegia 30 HRD220 SPG30
Hereditary Spastic Paraplegia 35 HRD227 FAHN
Hereditary Spastic Paraplegia 49 HRD226 SPG49
Hereditary Spastic Paraplegia 51 HRD186 CPSQ4
Hereditary Spastic Paraplegia 56 HRD229 SPG56
Hereditary Spastic Paraplegia 72 HRD188 SPG72
Hereditary Spherocytosis HRD011 HS
Hereditary Stomatocytosis HRD218
Hereditary Wilms' Tumor HRD009 WT1
Heritable Pulmonary Arterial Hypertension HRT015 FPAH
Heritable Thoracic Aortic Disease HRT036
Hermansky-Pudlak Syndrome HRM001 HPS
Hermansky-Pudlak Syndrome 1 HRM005 HPS1
Hermansky-Pudlak Syndrome 10 HRM020 HPS10
Hermansky-Pudlak Syndrome 11 HRM023 HPS11
Hermansky-Pudlak Syndrome 2 HRM017 HPS2
Hermansky-Pudlak Syndrome 3 HRM006 HPS3
Hermansky-Pudlak Syndrome 4 HRM007 HPS4
Hermansky-Pudlak Syndrome 5 HRM008 HPS5
Hermansky-Pudlak Syndrome 6 HRM009 HPS6
Hermansky-Pudlak Syndrome 7 HRM010 HPS7
Hermansky-Pudlak Syndrome 8 HRM011 HPS8
Hermansky-Pudlak Syndrome 9 HRM012 HPS9
Hermansky-Pudlak Syndrome Due to Ap-3 Deficiency HRM024
Hermansky-Pudlak Syndrome Due to Bloc-1 Deficiency HRM025
Hermansky-Pudlak Syndrome Due to Bloc-2 Deficiency HRM026
Hermansky-Pudlak Syndrome Due to Bloc-3 Deficiency HRM027
Hermaphroditism HRM002
Hernia, Hiatus HRN026
Heroin Dependence HRN003
Herpangina HRP001
Herpes Simplex HRP006
Herpes Simplex Encephalitis HRP009 HSE
Herpes Simplex Virus Keratitis HRP025
Herpes Zoster HRP004
Herpes Zoster Ophthalmicus HRP011 HZO
Herpes Zoster Oticus HRP037
Herpetic Whitlow HRP005
Herpetiform Pemphigus HRP026
Heterochromia Iridis HTR005
Heterophyiasis HTR001
Heterotaxy, Visceral, 1, X-Linked HTR014 HTX1
Heterotaxy, Visceral, 10, Autosomal, with Male Infertility HTR027 HTX10
Heterotaxy, Visceral, 11, Autosomal, with Male Infertility HTR028 HTX11
Heterotaxy, Visceral, 12, Autosomal HTR029 HTX12
Heterotaxy, Visceral, 2, Autosomal HTR009 HTX2
Heterotaxy, Visceral, 3, Autosomal HTR012 HTX3
Heterotaxy, Visceral, 4, Autosomal HTR010 HTX4
Heterotaxy, Visceral, 5, Autosomal HTR021 HTX5
Heterotaxy, Visceral, 6, Autosomal HTR023 HTX6
Heterotaxy, Visceral, 7, Autosomal HTR018 HTX7
Heterotaxy, Visceral, 8, Autosomal HTR020 HTX8
Heterotaxy, Visceral, 9, Autosomal, with Male Infertility HTR026 HTX9
Heyn-Sproul-Jackson Syndrome HYN001 HESJAS
Hfe Hemochromatosis HFH002
Hiatt-Neu-Cooper Neurodevelopmental Syndrome HTT003 HINCONS
Hidradenitis HDR003
Hidradenitis Suppurativa HDR002
Hidradenoma HDR004
Hidrocystoma HDR001
Hidrotic Ectodermal Dysplasia 2 HDR007
High Bone Mass Osteogenesis Imperfecta HGH023
High Density Lipoprotein Cholesterol Level Quantitative Trait Locus 1 HGH033 HDLCQ1
High Density Lipoprotein Cholesterol Level Quantitative Trait Locus 12 HGH039 HDLCQ12
High Density Lipoprotein Cholesterol Level Quantitative Trait Locus 14 HGH032 HDLCQ14
High Density Lipoprotein Cholesterol Level Quantitative Trait Locus 2 HGH034 HDLCQ2
High Density Lipoprotein Cholesterol Level Quantitative Trait Locus 3 HGH035
High Density Lipoprotein Cholesterol Level Quantitative Trait Locus 4 HGH036
High Density Lipoprotein Cholesterol Level Quantitative Trait Locus 5 HGH037
High Density Lipoprotein Cholesterol Level Quantitative Trait Locus 6 HGH038 HDLCQ6
High Grade Ependymoma HGH044
High Grade Glioma HGH043
High Molecular Weight Kininogen Deficiency HGH020 HMWK DEFICIENCY
High Pressure Neurological Syndrome HGH001
High-Grade Astrocytoma HGH041
High-Grade B-Cell Lymphoma Double-Hit/triple-Hit HGH045
Hilar Lung Carcinoma HLR002
Hilar Lung Neoplasm HLR001
Hirata Disease HRT040
Hirschsprung Disease 1 HRS035 HSCR1
Hirschsprung Disease 2 HRS036 HSCR2
Hirschsprung Disease 3 HRS034 HSCR3
Hirschsprung Disease 4 HRS029 HSCR4
Hirschsprung Disease 5 HRS027 HSCR5
Hirschsprung Disease 6 HRS028 HSCR6
Hirschsprung Disease 7 HRS026 HSCR7
Hirschsprung Disease 8 HRS025 HSCR8
Hirschsprung Disease 9 HRS024 HSCR9
Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction HRS016 HCAD
Hist1h1e Syndrome HST024
Histidine Metabolism Disease HST007
Histidinemia HST006 HISTID
Histiocytic and Dendritic Cell Cancer HST008
Histiocytic Sarcoma HST016
Histiocytoid Hemangioma HST004
Histiocytoma, Angiomatoid Fibrous HST022 AFH
Histiocytosis HST010
Histiocytosis-Lymphadenopathy Plus Syndrome HST017 HLAS
Histone Mutated Tumor HST025
Histoplasmosis HST011
Histoplasmosis Meningitis HST005
Histoplasmosis Pericarditis HST003
Histoplasmosis Retinitis HST002
Histrionic Personality Disorder HST001
Hivep2-Related Intellectual Disability HVP001 MRD43
Hnf1b-Related Autosomal Dominant Tubulointerstitial Kidney Disease HNF003 MODY5
Hobnail Hemangioma HBN001
Hodgkin's Granuloma HDG004
Hodgkin's Lymphoma, Lymphocytic Depletion HDG003
Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance HDG002
Hodgkin's Lymphoma, Mixed Cellularity HDG005
Hodgkin's Lymphoma, Nodular Sclerosis HDG001
Hodgkin's Paragranuloma HDG006
Holocarboxylase Synthetase Deficiency HLC001 HLCS DEFICIENCY
Holoprosencephaly HLP001 HPE
Holoprosencephaly 1 HLP023 HPE1
Holoprosencephaly 11 HLP016 HPE11
Holoprosencephaly 12 with or Without Pancreatic Agenesis HLP031 HPE12
Holoprosencephaly 13, X-Linked HLP032 HPE13
Holoprosencephaly 14 HLP034 HPE14
Holoprosencephaly 2 HLP024 HPE2
Holoprosencephaly 3 HLP026 HPE3
Holoprosencephaly 4 HLP029 HPE4
Holoprosencephaly 5 HLP028 HPE5
Holoprosencephaly 6 HLP021 HPE6
Holoprosencephaly 7 HLP027 HPE7
Holoprosencephaly 8 HLP022 HPE8
Holoprosencephaly 9 HLP025 HPE9
Holoprosencephaly, Recurrent Infections, and Monocytosis HLP004
Holt-Oram Syndrome HLT001 HOS
Holzgreve Syndrome HLZ001
Homocarnosinosis HMC001 SPG11
Homocysteinemia HMC014
Homocystinuria HMC002
Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency HMC030
Homocystinuria Due to Cystathionine Beta-Synthase Deficiency HMC040 CBSD
Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity HMC041 MTHFRD
Homocystinuria Without Methylmalonic Aciduria HMC036
Homocystinuria-Megaloblastic Anemia Cble Type HMC043 HMAE
Homocystinuria-Megaloblastic Anemia, Cble Complementation Type HMC042 HMAE
Homocystinuria-Megaloblastic Anemia, Cblg Complementation Type HMC033 HMAG
Homozygous 11p15-P14 Deletion Syndrome HMZ004
Homozygous Familial Hypercholesterolemia HMZ003 HOFH
Hordeolum HRD022 STYE
Hordeolum Externum HRD017 STYE
Hormone Producing Pituitary Cancer HRM003
Horner's Syndrome HRN001
Hot Water Epilepsy HTW002
Hot Water Reflex Epilepsy HTW001
Hoyeraal Hreidarsson Syndrome HYR002
Hsd10 Mitochondrial Disease HSD004 HSD10MD
Htra1-Related Cerebral Small Vessel Disease HTR024
Human Coronavirus Sensitivity HMN038 HCVS
Human Cytomegalovirus Infection HMN047
Human Granulocytic Anaplasmosis HMN002 HGE
Human Herpesvirus 8 HMN032 HHV8S
Human Immunodeficiency Virus Infectious Disease HMN014
Human Immunodeficiency Virus Type 1 HMN044 AIDS
Human Monocytic Ehrlichiosis HMN001 HME
Human Papillomavirus Infectious Disease HMN048 HPV
Human T-Cell Leukemia Virus Type 1 HMN021
Humerofemoral Hypoplasia with Radiotibial Ray Deficiency HMR045 HHRRD
Humeroradial Synostosis HMR015
Huntington Disease HNT016 HD
Huntington Disease-Like 1 HNT010 HDL1
Huntington Disease-Like 2 HNT004 HDL2
Huntington Disease-Like 3 HNT011 HDL3
Huntington Disease-Like Syndrome HNT013
Huntington Disease-Like Syndrome Due to C9orf72 Expansions HNT014
Huriez Syndrome HRZ001 HRZ
Hurler Syndrome HRL003 MPS1H
Hurler-Scheie Syndrome HRL004 MPS1H/S
Hutchinson-Gilford Progeria Syndrome HTC003 HGPS
Hyaline Body Myopathy HYL005
Hyaline Fibromatosis Syndrome HYL004 HFS
Hydatidiform Mole, Recurrent, 1 HYD046 HYDM1
Hydatidiform Mole, Recurrent, 2 HYD041 HYDM2
Hydatidiform Mole, Recurrent, 3 HYD067 HYDM3
Hydatidiform Mole, Recurrent, 4 HYD068 HYDM4
Hydranencephaly HYD001
Hydrarthrosis HYD003
Hydrocele HYD005
Hydrocephalus HYD006
Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius HYD019 HSAS
Hydrocephalus with Stenosis of the Aqueduct of Sylvius HYD048 HSAS
Hydrocephalus, Congenital Communicating, 1 HYD070 HYDCC1
Hydrocephalus, Congenital, 1 HYD064 HYC1
Hydrocephalus, Congenital, 2, with or Without Brain or Eye Anomalies HYD065 HYC2
Hydrocephalus, Congenital, 3, with Brain Anomalies HYD066 HYC3
Hydrocephalus, Normal-Pressure, 1 HYD071 HYDNP1
Hydrolethalus Syndrome 1 HYD033 HLS1
Hydrolethalus Syndrome 2 HYD040 HLS2
Hydromyelia HYD034
Hydronephrosis HYD002
Hydrophthalmos HYD007
Hydrops Fetalis, Nonimmune HYD038 NIHF
Hydrops of Gallbladder HYD004
Hydrops, Lactic Acidosis, and Sideroblastic Anemia HYD058 HLASA
Hydroxyacyl Glutathione Hydrolase Deficiency HYD063
Hydroxykynureninuria HYD030 HYXKY
Hymenolepiasis HYM001
Hyper Ige Recurrent Infection Syndrome 1 HYP847
Hyper Ige Recurrent Infection Syndrome 2 HYP861
Hyper Ige Recurrent Infection Syndrome 3 HYP862
Hyper Ige Recurrent Infection Syndrome 4 HYP863
Hyper Ige Syndrome HYP458 HIES
Hyperaldosteronism, Familial, Type I HYP731 HALD1
Hyperaldosteronism, Familial, Type Ii HYP600 HALD2
Hyperaldosteronism, Familial, Type Iii HYP438 HALD3
Hyperaldosteronism, Familial, Type Iv HYP708 HALD4
Hyperalphalipoproteinemia 1 HYP732 HALP1
Hyperandrogenism HYP043
Hyperandrogenism Due to Cortisone Reductase Deficiency HYP625
Hyperbilirubinemia, Rotor Type HYP236 HBLRR
Hyperbilirubinemia, Transient Familial Neonatal HYP766 HBLRTFN
Hyperbiliverdinemia HYP481 HBLVD
Hypercalcemia, Infantile, 1 HYP726 HCINF1
Hypercalcemia, Infantile, 2 HYP712 HCINF2
Hypercalciuria, Absorptive, 1 HYP809 HCA1
Hypercalciuria, Absorptive, 2 HYP733 HCA2
Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant HYP276 HCVAD
Hypercementosis HYP021
Hyperchlorhidrosis, Isolated HYP267 HYCHL
Hypercholanemia, Familial 1 HYP872 FHCA1
Hypercholanemia, Familial, 2 HYP873 FHCA2
Hypercholesterolemia Due to Cholesterol 7alpha-Hydroxylase Deficiency HYP485
Hypercholesterolemia, Familial, 1 HYP836 FHCL1
Hypercholesterolemia, Familial, 2 HYP837 FHCL2
Hypercholesterolemia, Familial, 3 HYP272 FHCL3
Hypercholesterolemia, Familial, 4 HYP840 FHCL4
Hyperekplexia HYP097 STHE
Hyperekplexia 1 HYP699 HKPX1
Hyperekplexia 2 HYP510 HKPX2
Hyperekplexia 3 HYP519 HKPX3
Hyperekplexia 4 HYP825 HKPX4
Hypereosinophilic Syndrome HYP098 HES
Hypereosinophilic Syndrome, Idiopathic HYP810 HES
Hyperferritinemia with or Without Cataract HYP801 HRFTC
Hyperglobulinemic Purpura HYP018
Hyperglycemia HYP066
Hyperglycinemia, Lactic Acidosis, and Seizures HYP719 HGCLAS
Hyperglycinuria HYP348 HG
Hyperhidrosis Palmaris Et Plantaris HYP560 HYPRPP
Hyperhidrosis, Gustatory HYP737 HYPRG
Hyperhomocysteinemia HYP037
Hyper-Igd Syndrome HYP088 HIDS
Hyper-Ige Recurrent Infection Syndrome 1, Autosomal Dominant HYP828 HIES1
Hyper-Ige Recurrent Infection Syndrome 2, Autosomal Recessive HYP829 HIES2
Hyper-Ige Recurrent Infection Syndrome 3, Autosomal Recessive HYP833 HIES3
Hyper-Ige Recurrent Infection Syndrome 4a, Autosomal Dominant HYP885 HIES4A
Hyper-Ige Recurrent Infection Syndrome 4b, Autosomal Recessive HYP884 HIES4B
Hyper-Ige Recurrent Infection Syndrome 5, Autosomal Recessive HYP871 HIES5
Hyperinsulinemic Hypoglycemia HYP050
Hyperinsulinemic Hypoglycemia, Familial, 1 HYP304 HHF1
Hyperinsulinemic Hypoglycemia, Familial, 2 HYP604 HHF2
Hyperinsulinemic Hypoglycemia, Familial, 3 HYP601 HHF3
Hyperinsulinemic Hypoglycemia, Familial, 4 HYP271 HHF4
Hyperinsulinemic Hypoglycemia, Familial, 5 HYP326 HHF5
Hyperinsulinemic Hypoglycemia, Familial, 6 HYP807 HHF6
Hyperinsulinemic Hypoglycemia, Familial, 7 HYP349 HHF7
Hyperinsulinism HYP060
Hyperinsulinism Due to Hnf1a Deficiency HYP490
Hyperinsulinism Due to Hnf4a Deficiency HYP479
Hyperinsulinism Due to Ucp2 Deficiency HYP482
Hyperkalemic Periodic Paralysis HYP052 HYPP
Hyperkeratosis Lenticularis Perstans HYP160 HLP
Hyperleucine-Isoleucinemia HYP240
Hyperlipidemia, Familial Combined, 1 HYP839 FCHL1
Hyperlipidemia, Familial Combined, 2 HYP842 FCHL2
Hyperlipidemia, Familial Combined, 3 HYP838 FCHL3
Hyperlipoproteinemia, Type I HYP768 HLPP1
Hyperlipoproteinemia, Type Id HYP819 HLPP1D
Hyperlipoproteinemia, Type Iii HYP724 CAD
Hyperlipoproteinemia, Type Iv HYP739
Hyperlipoproteinemia, Type V HYP740 HLPP5
Hyperlucent Lung HYP015
Hyperlysinemia, Type I HYP769 HYPLYS1
Hypermanganesemia with Dystonia HYP821
Hypermanganesemia with Dystonia 1 HYP716 HMNDYT1
Hypermanganesemia with Dystonia 2 HYP713 HMNDYT2
Hypermethioninemia HYP003 MET
Hypermethioninemia Due to Adenosine Kinase Deficiency HYP241 HMAKD
Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency HYP814 HMAHCHD
Hypermobile Ehlers-Danlos Syndrome HYP706 EDS3
Hypermobility of Coccyx HYP010
Hypermobility Syndrome HYP007
Hyperopia, High HYP773
Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome HYP774 HHHS
Hyperostosis HYP068
Hyperostosis Cranialis Interna HYP674 HCIN
Hyperoxaluria, Primary, Type I HYP794 HP1
Hyperoxaluria, Primary, Type Ii HYP602 HP2
Hyperoxaluria, Primary, Type Iii HYP603 HP3
Hyperparathyroidism HYP069
Hyperparathyroidism 1 HYP243 HRPT1
Hyperparathyroidism 2 with Jaw Tumors HYP741 HRPT2
Hyperparathyroidism 3 HYP311 HRPT3
Hyperparathyroidism 4 HYP720 HRPT4
Hyperparathyroidism, Neonatal Severe HYP776 NSHPT
Hyperparathyroidism, Transient Neonatal HYP831 HRPTTN
Hyperphalangy HYP497
Hyperphenylalaninemia HYP141
Hyperphenylalaninemia, Bh4-Deficient, a HYP331 HPABH4A
Hyperphenylalaninemia, Bh4-Deficient, B HYP605 HPABH4B
Hyperphenylalaninemia, Bh4-Deficient, C HYP368 HPABH4C
Hyperphenylalaninemia, Bh4-Deficient, D HYP365 HPABH4D
Hyperphenylalaninemia, Mild, Non-Bh4-Deficient HYP722 HPANBH4
Hyperphosphatasia with Mental Retardation Syndrome 1 HYP441 HPMRS1
Hyperphosphatasia with Mental Retardation Syndrome 2 HYP442 HPMRS2
Hyperphosphatasia with Mental Retardation Syndrome 3 HYP553 HPMRS3
Hyperphosphatasia with Mental Retardation Syndrome 4 HYP580 HPMRS4
Hyperphosphatasia with Mental Retardation Syndrome 6 HYP697 HPMRS6
Hyperphosphatasia-Intellectual Disability Syndrome HYP629
Hyperphosphatemia HYP025
Hyperpigmentation of the Skin HYP855
Hyperpigmentation with or Without Hypopigmentation, Familial Progressive HYP744 FPHH
Hyperpigmentation, Familial Progressive, 1 HYP563 FPH1
Hyperpituitarism HYP070
Hyperproinsulinemia HYP110 HPRI
Hyperprolactinemia HYP020 HPRL
Hyperprolinemia HYP111
Hyperprolinemia, Type I HYP248 HYRPRO1
Hyperprolinemia, Type Ii HYP597 HYRPRO2
Hypersensitivity Reaction Type Iii Disease HYP072
Hypersensitivity Reaction Type Iv Disease HYP073
Hypersensitivity Vasculitis HYP074
Hypersomnia HYP263
Hypersplenism HYP063
Hypertelorism HYP748
Hypertelorism and Tetralogy of Fallot HYP176
Hypertelorism, Microtia, Facial Clefting Syndrome HYP059
Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness HYP561 HPPD
Hypertension and Brachydactyly Syndrome HYP648 HTNB
Hypertension Due to Gain-of-Function Mutations in the Mineralocorticoid Receptor HYP869
Hypertension, Diastolic HYP540
Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy HYP806 EOHSEP
Hypertension, Essential HYP595 EHT
Hypertension, Essential 1 HYP447 HYT1
Hypertension, Essential 2 HYP448 HYT2
Hypertension, Essential 3 HYP449 HYT3
Hypertension, Essential 4 HYP450 HYT4
Hypertension, Essential 5 HYP451 HYT5
Hypertension, Essential 6 HYP452 HYT6
Hypertension, Essential 7 HYP453 HYT7
Hypertension, Essential 8 HYP454 HYT8
Hypertensive Encephalopathy HYP034
Hypertensive Heart Disease HYP006
Hypertensive Nephropathy HYP114 HNP1
Hypertensive Retinopathy HYP008
Hyperthyroidism HYP076
Hyperthyroidism, Familial Gestational HYP344 HTFG
Hyperthyroidism, Nonautoimmune HYP249 HTNA
Hyperthyroxinemia HYP029
Hyperthyroxinemia, Dystransthyretinemic HYP645 DTTRH
Hyperthyroxinemia, Familial Dysalbuminemic HYP677 FDAH
Hypertonia HYP264
Hypertrichosis HYP077
Hypertrichosis Universalis Congenita, Ambras Type HYP351 HTC1
Hypertrichosis, Congenital Generalized, with or Without Gingival Hyperplasia HYP728 HTC3
Hypertriglyceridemia 1 HYP875 HYTG1
Hypertriglyceridemia 2 HYP876 HYTG2
Hypertriglyceridemia, Transient Infantile HYP555 HTGTI
Hypertrophic Cardiomyopathy HYP061
Hypertrophic Cardiomyopathy with Kidney Anomalies Due to Mitochondrial Dna Mutation HYP887
Hypertrophic Neuropathy of Dejerine-Sottas HYP186 DSS
Hypertrophic Osteoarthropathy, Primary, Autosomal Dominant HYP759 PHOAD
Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 HYP793 PHOAR1
Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 2 HYP520 PHOAR2
Hypertrophic Pyloric Stenosis HYP009
Hypertrophic Scars HYP457
Hypertrophy of Breast HYP078
Hypertrophy of Tongue Papillae HYP049
Hypertropia HYP047
Hypertryptophanemia HYP187 HYPTRP
Hyperuricemia HYP014
Hyperuricemia, Hprt-Related HYP870 HRH
Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome HYP815 HUPRAS
Hyperuricemic Nephropathy, Familial Juvenile, 3 HYP529 HNFJ3
Hypervalinemia and Hyperleucine-Isoleucinemia HYP866 HVLI
Hypervitaminosis a HYP058
Hypervitaminosis D HYP057
Hypoactive Sexual Desire Disorder HYP030
Hypoadrenocorticism, Familial HYP780
Hypoaldosteronism HYP120
Hypoalphalipoproteinemia HYP121
Hypoalphalipoproteinemia, Primary, 1 HYP841 FHA1
Hypoalphalipoproteinemia, Primary, 2 HYP843 FHA2
Hypoalphalipoproteinemia, Primary, 2, Intermediate HYP886 FHA2I
Hypoascorbemia HYP781
Hypobetalipoproteinemia, Familial, 1 HYP818 FHBL1
Hypobetalipoproteinemia, Familial, 2 HYP290 FHBL2
Hypocalcemia, Autosomal Dominant 1 HYP802 HYPOC1
Hypocalcemia, Autosomal Dominant 2 HYP564 HYPOC2
Hypocalcemic Vitamin D-Dependent Rickets HYP636 VDDI
Hypocalciuric Hypercalcemia, Familial, Type I HYP752 HHC1
Hypocalciuric Hypercalcemia, Familial, Type Ii HYP753 HHC2
Hypocalciuric Hypercalcemia, Familial, Type Iii HYP608 HHC3
Hypochondriasis HYP016
Hypochondrogenesis HYP041
Hypochondroplasia HYP042 HCH
Hypochromic Microcytic Anemia HYP001
Hypocomplementemic Urticarial Vasculitis HYP193
Hypofibrinogenemia, Familial HYP197
Hypoganglionosis HYP572
Hypoglossal Nerve Disease HYP028
Hypoglycemia HYP056
Hypoglycemia, Leucine-Induced HYP782 LIH
Hypoglycemic Coma HYP026
Hypogonadism HYP080
Hypogonadism, Male HYP784
Hypogonadotropic Hypogonadism HYP730
Hypogonadotropic Hypogonadism 1 with or Without Anosmia HYP513 HH1
Hypogonadotropic Hypogonadism 10 with or Without Anosmia HYP521 HH10
Hypogonadotropic Hypogonadism 11 with or Without Anosmia HYP522 HH11
Hypogonadotropic Hypogonadism 12 with or Without Anosmia HYP547 HH12
Hypogonadotropic Hypogonadism 13 with or Without Anosmia HYP443 HH13
Hypogonadotropic Hypogonadism 14 with or Without Anosmia HYP523 HH14
Hypogonadotropic Hypogonadism 15 with or Without Anosmia HYP511 HH15
Hypogonadotropic Hypogonadism 16 with or Without Anosmia HYP518 HH16
Hypogonadotropic Hypogonadism 17 with or Without Anosmia HYP538 HH17
Hypogonadotropic Hypogonadism 18 with or Without Anosmia HYP532 HH18
Hypogonadotropic Hypogonadism 19 with or Without Anosmia HYP557 HH19
Hypogonadotropic Hypogonadism 2 with or Without Anosmia HYP548 HH2
Hypogonadotropic Hypogonadism 20 with or Without Anosmia HYP546 HH20
Hypogonadotropic Hypogonadism 21 with or Without Anosmia HYP817 HH21
Hypogonadotropic Hypogonadism 22 with or Without Anosmia HYP820 HH22
Hypogonadotropic Hypogonadism 23 with or Without Anosmia HYP651 HH23
Hypogonadotropic Hypogonadism 24 with or Without Anosmia HYP881 HH24
Hypogonadotropic Hypogonadism 25 with Anosmia HYP865 HH25
Hypogonadotropic Hypogonadism 26 with or Without Anosmia HYP882 HH26
Hypogonadotropic Hypogonadism 27 Without Anosmia HYP883 HH27
Hypogonadotropic Hypogonadism 3 with or Without Anosmia HYP565 HH3
Hypogonadotropic Hypogonadism 4 with or Without Anosmia HYP531 HH4
Hypogonadotropic Hypogonadism 5 with or Without Anosmia HYP549 HH5
Hypogonadotropic Hypogonadism 6 with or Without Anosmia HYP552 HH6
Hypogonadotropic Hypogonadism 7 with or Without Anosmia HYP535 HH7
Hypogonadotropic Hypogonadism 8 with or Without Anosmia HYP514 HH8
Hypogonadotropic Hypogonadism 9 with or Without Anosmia HYP444 HH9
Hypohidrotic Ectodermal Dysplasia Autosomal Recessive HYP206
Hypohidrotic Ectodermal Dysplasia with Immunodeficiency HYP643
Hypoinsulinemic Hypoglycemia with Hemihypertrophy HYP524 HIHGHH
Hypokalemia HYP005
Hypokalemic Periodic Paralysis, Type 1 HYP370 HOKPP1
Hypokalemic Periodic Paralysis, Type 2 HYP606 HOKPP2
Hypokalemic Tubulopathy and Deafness HYP877 HKTD
Hypolipoproteinemia HYP081
Hypomagnesemia 1, Intestinal HYP550 HOMG1
Hypomagnesemia 2, Renal HYP210 HOMG2
Hypomagnesemia 3, Renal HYP534 HOMG3
Hypomagnesemia 4, Renal HYP302 HOMG4
Hypomagnesemia 5, Renal, with or Without Ocular Involvement HYP827 HOMG5
Hypomagnesemia 6, Renal HYP445 HOMG6
Hypomagnesemia, Hypertension, and Hypercholesterolemia, Mitochondrial HYP800
Hypomagnesemia, Seizures, and Mental Retardation 1 HYP830 HOMGSMR1
Hypomagnesemia, Seizures, and Mental Retardation 2 HYP834 HOMGSMR2
Hypomelanosis of Ito HYP691 HMI
Hypomyelinating Leukodystrophy HYP700 HLD
Hypomyelinating Leukoencephalopathy HYP659
Hypomyelination Neuropathy-Arthrogryposis Syndrome HYP671
Hypomyelination of Early Myelinating Structures HYP878 HEMS
Hypomyelination with Brainstem and Spinal Cord Involvement and Leg Spasticity HYP530 HBSL
Hypoparathyroidism HYP024
Hypoparathyroidism, Familial Isolated, 1 HYP864 FIH1
Hypoparathyroidism, Familial Isolated, 2 HYP867 FIH2
Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome HYP880 HDRS
Hypoparathyroidism, X-Linked HYP611 HYPX
Hypoparathyroidism-Deafness-Renal Disease Syndrome HYP666
Hypoparathyroidism-Retardation-Dysmorphism Syndrome HYP134 HRDS
Hypopharynx Cancer HYP082
Hypophosphatasia HYP035 HPP
Hypophosphatasia, Adult HYP293 HPPA
Hypophosphatasia, Childhood HYP596 HPPC
Hypophosphatasia, Infantile HYP292 HPPI
Hypophosphatemia HYP017 VDRR
Hypophosphatemic Bone Disease HYP754 HBD
Hypophosphatemic Nephrolithiasis/osteoporosis HYP868
Hypophosphatemic Rickets and Hyperparathyroidism HYP312
Hypophosphatemic Rickets with Hypercalciuria, Hereditary HYP789 HHRH
Hypophosphatemic Rickets, Autosomal Dominant HYP260 ADHR
Hypophosphatemic Rickets, Autosomal Recessive, 1 HYP788 ARHR1
Hypophosphatemic Rickets, Autosomal Recessive, 2 HYP369 ARHR2
Hypophosphatemic Rickets, X-Linked Dominant HYP609 XLHR
Hypophosphatemic Rickets, X-Linked Recessive HYP798 XLRHR
Hypopigmentation of Eyelid HYP046
Hypopigmentation of the Skin HYP854
Hypopigmentation, Organomegaly, and Delayed Myelination and Development HYP846 HOD
Hypopituitarism HYP083
Hypoplastic Amelogenesis Imperfecta HYP658
Hypoplastic Femurs and Pelvis HYP879 HYPOFP
Hypoplastic Left Heart Syndrome HYP055 HLHS
Hypoplastic Left Heart Syndrome 1 HYP543 HLHS1
Hypoplastic Left Heart Syndrome 2 HYP517 HLHS2
Hypoplastic Pancreas-Intestinal Atresia-Hypoplastic Gallbladder Syndrome HYP848
Hypoplastic Right Heart Syndrome HYP223
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, and Pallidal Degeneration HYP808 HARP
Hypopyon HYP084
Hypopyon Ulcer HYP062
Hypospadias HYP040
Hypospadias 1, X-Linked HYP284 HYSP1
Hypospadias 2, X-Linked HYP270 HYSP2
Hypospadias 3, Autosomal HYP545 HYSP3
Hypospadias 4, X-Linked HYP653 HYSP4
Hypotaurinemic Retinal Degeneration and Cardiomyopathy HYP874 HTRDC
Hypothalamic Disease HYP085
Hypothalamic Neoplasm HYP002
Hypothyroidism HYP086
Hypothyroidism Due to Deficient Transcription Factors Involved in Pituitary Development or Function HYP488
Hypothyroidism, Central, with Testicular Enlargement HYP856 CHTE
Hypothyroidism, Congenital, Nongoitrous, 1 HYP374 CHNG1
Hypothyroidism, Congenital, Nongoitrous, 2 HYP760 CHNG2
Hypothyroidism, Congenital, Nongoitrous, 3 HYP355 CHNG3
Hypothyroidism, Congenital, Nongoitrous, 4 HYP795 CHNG4
Hypothyroidism, Congenital, Nongoitrous, 5 HYP762 CHNG5
Hypothyroidism, Congenital, Nongoitrous, 6 HYP562 CHNG6
Hypothyroidism, Congenital, Nongoitrous, 7 HYP860 CHNG7
Hypothyroidism, Congenital, Nongoitrous, 8 HYP857 CHNG8
Hypothyroidism, Congenital, Nongoitrous, 9 HYP858 CHNG9
Hypothyroidism, Thyroidal or Athyroidal, with Spiky Hair and Cleft Palate HYP791 BLS
Hypotonia HYP265
Hypotonia, Ataxia, and Delayed Development Syndrome HYP711 HADDS
Hypotonia, Ataxia, Developmental Delay, and Tooth Enamel Defect Syndrome HYP823 HADDTS
Hypotonia, Hypoventilation, Impaired Intellectual Development, Dysautonomia, Epilepsy, and Eye Abnormalities HYP859 HIDEA
Hypotonia, Infantile, with Psychomotor Retardation HYP717 IHPMR
Hypotonia, Infantile, with Psychomotor Retardation and Characteristic Facies 1 HYP723 IHPRF1
Hypotonia, Infantile, with Psychomotor Retardation and Characteristic Facies 2 HYP698 IHPRF2
Hypotonia, Infantile, with Psychomotor Retardation and Characteristic Facies 3 HYP714 IHPRF3
Hypotonia-Cystinuria Syndrome HYP347 HCS
Hypotonia-Speech Impairment-Severe Cognitive Delay Syndrome HYP638
Hypotrichosis HYP087
Hypotrichosis 1 HYP507 HYPT1
Hypotrichosis 10 HYP544 HYPT10
Hypotrichosis 11 HYP528 HYPT11
Hypotrichosis 12 HYP578 HYPT12
Hypotrichosis 13 HYP577 HYPT13
Hypotrichosis 14 HYP832 HYPT14
Hypotrichosis 2 HYP525 HYPT2
Hypotrichosis 3 HYP515 HYPT3
Hypotrichosis 4 HYP576 HYPT4
Hypotrichosis 5 HYP573 HYPT5
Hypotrichosis 6 HYP581 HYPT6
Hypotrichosis 7 HYP575 HYPT7
Hypotrichosis 8 HYP559 HYPT8
Hypotrichosis 9 HYP551 HYPT9
Hypotrichosis and Recurrent Skin Vesicles HYP346 HYPTSV
Hypotrichosis Simplex HYP137 HHS
Hypotrichosis Simplex of the Scalp HYP641
Hypotrichosis, Congenital, with Juvenile Macular Dystrophy HYP332 HJMD
Hypotrichosis-Lymphedema-Telangiectasia Syndrome HYP139 HLTS
Hypotrichosis-Lymphedema-Telangiectasia-Renal Defect Syndrome HYP652 HLTRS
Hypotropia HYP048
Hypouricemia, Renal, 1 HYP761 RHUC1
Hypouricemia, Renal, 2 HYP376 RHUC2
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