Select item 42397 HbH hemoglobin Select item 468531 Hemoglobin H disease ALPHA-THALASSEMIA, HEMOGLOBIN H TYPE HEMOGLOBIN H DISEASE, DELETIONAL Select item 395255 Bombay phenotype Select item 400532 H syndrome Asrar Facharzt Haque syndrome Faisalabad histiocytosis HISTIOCYTOSIS AND LYMPHADENOPATHY WITH OR WITHOUT CUTANEOUS, CARDIAC, AND/OR ENDOCRINE FEATURES, JOINT CONTRACTURES, AND/OR DEAFNESS HYPERPIGMENTATION, CUTANEOUS, WITH HYPERTRICHOSIS, HEPATOSPLENOMEGALY, HEART ANOMALIES, AND HYPOGONADISM WITH OR WITHOUT HEARING LOSS Histiocytosis with joint contractures and sensorineural deafness Histiocytosis-lymphadenopathy plus syndrome Hyperpigmentation, Cutaneous, with Hypertrichosis, Hepatosplenomegaly, Heart Anomalies, Hearing Loss, and Hypogonadism PIGMENTED HYPERTRICHOSIS WITH INSULIN-DEPENDENT DIABETES MELLITUS Pigmented hypertrichosis and insulin-dependent diabetes mellitus ROSAI-DORFMAN DISEASE, FAMILIAL SINUS HISTIOCYTOSIS AND MASSIVE LYMPHADENOPATHY Select item 462293 Long QT syndrome 2 Select item 1635567 Adams-Oliver syndrome 1 ABSENCE DEFECT OF LIMBS, SCALP, AND SKULL APLASIA CUTIS CONGENITA WITH TERMINAL TRANSVERSE LIMB DEFECTS Aplasia cutis congenita with terminal transverse defects of limbs, and skull defects CONGENITAL SCALP DEFECTS WITH DISTAL LIMB REDUCTION ANOMALIES Forrest H Adams syndrome Scalp and head syndrome Scalp defects with ectrodactyly Select item 108433 Acquired hemoglobin H disease Alpha-thalassemia myelodysplasia syndrome Alpha-thalassemia myelodysplasia syndrome, somatic Alpha-thalassemia-myelodysplastic syndrome Select item 75656 Xeroderma pigmentosum, group D ERCC2-Related Xeroderma Pigmentosum XERODERMA PIGMENTOSUM IV XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D XP, GROUP D XP, GROUP H XP4 XERODERMA PIGMENTOSUM VIII Select item 96024 Factor H deficiency CFH DEFICIENCY COMPLEMENT FACTOR H DEFICIENCY Select item 44193 Long QT syndrome Select item 355891 Short QT syndrome type 1 Select item 1434 alpha Thalassemia A-Thalassemia Alpha thalassemia spectrum Select item 65123 X-linked agammaglobulinemia AGAMMAGLOBULINEMIA, X-LINKED, TYPE 1 Agammaglobulinemia, BTK Agammaglobulinemia, Bruton tyrosine kinase BTK-deficiency Bruton's agammaglobulinemia Bruton-type agammaglobulinemia IMMUNODEFICIENCY 1 Select item 162892 Alpha thalassemia-intellectual disability syndrome type 1 ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, DELETION-TYPE ATR, DELETION-TYPE ATR-16 SYNDROME CHROMOSOME 16p DELETION SYNDROME Chromosome 16-related alpha-thalassemia/mental retardation syndrome HEMOGLOBIN H-RELATED MENTAL RETARDATION MENTAL RETARDATION WITH HEMOGLOBIN H Select item 543726 Hemoglobin Bart hydrops syndrome Alpha thalassemia major Hb Bart Hb Bart's hydrops fetalis Hemoglobin Bart's hydrops syndrome Hydrops fetalis, alpha-thalassemia-related Select item 376400 VACTERL with hydrocephalus VACTERL association with hydrocephalus VACTERL-H Select item 374443 Hypoparathyroidism, deafness, renal disease syndrome Barakat syndrome HDR syndrome HYPOPARATHYROIDISM, SENSORINEURAL DEAFNESS, AND RENAL DYSPLASIA SYNDROME Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypoparathyroidism, sensorineural deafness, and renal dysplasia Nephrosis, nerve deafness, and hypoparathyroidism Select item 409919 Glaucoma 1, open angle, H Select item 472581 Omeprazole response OMEPRAZOLE, POOR METABOLISM OF Prilosec response Select item 450454 Esomeprazole response 
