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List of all diseases starting with H

• HAREL-YOON SYNDROME (HAYOS) MIM=617183
• HARTNUP DISEASE (HND) MIM=234500
• HAWKINSINURIA MIM=140350
• HEARING LOSS [DD] MIM=
• HEMOCHROMATOSIS, NEONATAL MIM=231100
• HEMOCHROMATOSIS, TYPE 1 MIM=235200
• HEMOCHROMATOSIS, TYPE 2A MIM=602390
• HEMOCHROMATOSIS, TYPE 2B MIM=613313
• HEMOCHROMATOSIS, TYPE 3 MIM=604250
• HEMOCHROMATOSIS, TYPE 4 MIM=606069
• HEMOCHROMATOSIS, TYPE 5 MIM=615517
• HEMOLYTIC ANEMIA DUE TO GLUTATHIONE REDUCTASE DEFICIENCY MIM=618660
• HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY (GPI) MIM=613470
• HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY (HK1) MIM=235700
• HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1 MIM=267700
• HEPATIC LIPASE DEFICIENCY MIM=614025
• HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 6 (HDLCQ6) MIM=610762
• HISTIDINEMIA MIM=235800
• HISTIDINURIA MIM=235830
• HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME MIM=602782
• HOMOCARNOSINOSIS MIM=236130
• HOMOCYSTINURIA DUE TO DEFECT OF N(5,10)-METHYLENE THF DEFICIENCY (MTHFR) MIM=236250
• HOMOCYSTINURIA, CYSTATHIONINE BETA-SYNTHASE DEFICIENCY (CBS) MIM=236200
• HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA DUE TO DEFECT IN COBALAMIN METABOLISM, cblG COMPLEMENTATION TYPE MIM=250940
• HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, cblE COMPLEMENTATION TYPE (HMAE) MIM=236270
• HYDROPS FETALIS, NON IMMUNE MIM=236750
• HYDROPS, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA; (HLASA) MIM=617021
• HYDROXYKYNURENINURIA MIM=236800
• HYDROXYLYSINURIA MIM=236900
• HYDROXYPROLINEMIA MIM=237000
• HYPER BETA-ALANINEMIA MIM=237400
• HYPER-IgD SYNDROME MIM=260920
• HYPERALDOSTERONISM, FAMILIAL, TYPE I; HALD1 MIM=103900
• HYPERALDOSTERONISM, FAMILIAL, TYPE II; HALD2 MIM=605635
• HYPERALDOSTERONISM, FAMILIAL, TYPE III; HALD3 MIM=613677
• HYPERALPHALIPOPROTEINEMIA 1 (HALP1) MIM=143470
• HYPERAMMONEMIA, TRANSIENT, OF THE NEWBORN (THAN) MIM=---
• HYPERBILIRUBINEMIA, ROTOR TYPE (HBLRR) MIM=237450
• HYPERCAROTENEMIA AND VITAMIN A DEFICIENCY, AUTOSOMAL DOMINANT (HCVAD) MIM=115300
• HYPERCHOLANEMIA, FAMILIAL (FHCA) MIM=607748
• HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, TYPE B MIM=144010
• HYPERCHOLESTEROLEMIA, FAMILIAL, 1 (FHCL1) MIM=143890
• HYPERCHOLESTEROLEMIA, FAMILIAL, 3 (FHCL3) MIM=603776
• HYPERCHOLESTEROLEMIA, FAMILIAL, 4 (FHCL4) MIM=603813
• HYPERCYSTINURIA -> MOVED TO CYSTINURIA MIM=220100
• HYPEREKPLEXIA MIM=149400
• HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES; HGCLAS MIM=614462
• HYPERGLYCINEMIA, NON-KETOTIC (NKH) MIM=605899
• HYPERGLYCINURIA MIM=138500
• HYPERINSULINEMIC HYPOGLYCEMIA DUE TO UNCOUPLING PROTEIN 2; UCP2 MIM=601693
• HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1, HHF1 MIM=256450
• HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 2, HHF2 MIM=601820
• HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 3; HHF3 MIM=602485
• HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 4; HHF4 MIM=609975
• HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 5; HHF5 MIM=609968
• HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 6; HHF6 MIM=606762
• HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 7; HHF7 MIM=610021
• HYPERINSULINEMIC HYPOGLYCEMIA, TRANSIENT OR PERMANENT [DD] MIM=
• HYPERKYNURENINURIA MIM=236800
• HYPERLEUCINE-ISOLEUCINEMIA (BCAA) MIM=238340
• HYPERLIPOPROTEINEMIA, TYPE IV MIM=144600
• HYPERLYSINEMIA I, FAMILIAL MIM=238700
• HYPERLYSINEMIA II OR SACCHAROPINURIA MIM=268700
• HYPERLYSINURIA MIM=247950
• HYPERMANGANESEMIA WITH DYSTONIA 1 (HMNDYT1) MIM=613280
• HYPERMANGANESEMIA WITH DYSTONIA 2 (HMNDYT2) MIM=617013
• HYPERORNITHINEMIA WITH GYRATE ATROPHY (HOGA, OAT) MIM=258870
• HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA (HHH-SYNDROME) MIM=238970
• HYPEROXALURIA, PRIMARY, TYPE I, PH1 MIM=259900
• HYPEROXALURIA, PRIMARY, TYPE II, PH2 MIM=260000
• HYPEROXALURIA, PRIMARY, TYPE III, PH3 MIM=613616
• HYPERPHENYLALANIEMIA DUE TO GUANOSINE TRIPHOSPHATE CYCLOHYDROLASE DEFICIENCY MIM=233910
• HYPERPHENYLALANINEMIA DUE TO 6-PYRUVOYLTETRAHYDROPTERIN SYNTHASE DEFICIENCY (PTPS) MIM=261640
• HYPERPHENYLALANINEMIA DUE TO DHPR-DEFICIENCY (DHPR) MIM=261630
• HYPERPHENYLALANINEMIA DUE TO PTERIN-4a-CARBINOLAMINE DEHYDRATASE MIM=264070
• HYPERPHENYLALANINEMIA, MILD, NON-BH4-DEFICIENT (DNAJC12) MIM=617384
• HYPERPHOSPHATASIA (JPD) MIM=239000
• HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1; HPMRS1 MIM=239300
• HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6; HPMRS6 MIM=616809
• HYPERPIPECOLATEMIA MIM=239400
• HYPERPROLINEMIA, TYPE I MIM=239500
• HYPERPROLINEMIA, TYPE II MIM=239510
• HYPERTRIGLYCERIDEMIA, TRANSIENT INFANTILE (HTGTI, GPD1) MIM=614480
• HYPERTRYPTOPHANEMIA (HYPTRP) MIM=600627
• HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME; HUPRAS MIM=613845
• HYPERVALINEMIA MIM=277100
• HYPERZINCAEMIA AND HYPERCALPROTECTINAEMIA MIM=194470
• HYPERZINCEMIA WITH FUNCTIONAL ZINC DEPLETION MIM=601979
• HYPOADRENOCORTICISM, FAMILIAL MIM=240200
• HYPOBETALIPOPROTEINEMIA, FAMILIAL, 1 (FHBL1) MIM=615558
• HYPOBETALIPOPROTEINEMIA, FAMILIAL, 2 (FHBL2) MIM=615019
• HYPOGLYCEMIA, FAMILIAL NEONATAL MIM=240800
• HYPOINSULINEMIC HYPOGLYCEMIA WITH HEMIHYPERTROPHY; HIHGHH (AKT2) MIM=240900
• HYPOMAGNESEMIA 1, INTESTINAL; HOMG1 MIM=602014
• HYPOMAGNESEMIA 2, RENAL; HOMG2 MIM=154020
• HYPOMAGNESEMIA 3, RENAL; HOMG3 MIM=248250
• HYPOMAGNESEMIA 4, RENAL; HOMG4 MIM=611718
• HYPOMAGNESEMIA 5, RENAL, WITH OCULAR INVOLVEMENT; HOMG5 MIM=248190
• HYPOMAGNESEMIA 6, RENAL; HOMG6 MIM=613882
• HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION 1 (HOMGSMR1) MIM=616418
• HYPOPARATHYROIDISM, FAMILIAL ISOLATED; FIH MIM=146200
• HYPOPARATHYROIDISM, X-LINKED; HYPX MIM=307700
• HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME; HRDS MIM=241410
• HYPOPHOSPHATASIA, ADULT ; ODONTOHYPOPHOSPHATASIA MIM=146300
• HYPOPHOSPHATASIA, CHILDHOOD MIM=241510
• HYPOPHOSPHATASIA, INFANTILE MIM=241500
• HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT (XLHR) MIM=307800
• HYPOPIGMENTATION, ORGANOMEGALY, AND DELAYED MYELINATION AND DEVELOPMENT (HOD) MIM=618541
• HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1; CHNG1 MIM=275200
• HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2; CHNG2 MIM=218700
• HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 4; CHNG4 MIM=275100
• HYPOTONIA-CYSTINURIA SYNDROME MIM=606407
• HYPOURICEMIA, RENAL, 1 (RHUC1) MIM=220150
• HYPOURICEMIA, RENAL, 2 (RHUC2) MIM=612076