Medical Conditions — H
19 conditions found
Hallermann-Streiff syndromeQ87.0Heavy chain deposition diseaseD89.89Heme oxygenase-1 deficiencyD59.9Hemifacial myohyperplasiaQ87.0Hemoglobin C diseaseD58.2Hereditary angioedema with normal C1InhD84.1Hereditary hypercarotenemia and vitamin A deficiencyE50.8Hereditary isolated aplastic anemiaD61.09Hereditary renal hypouricemiaE79.0Hereditary sensory and autonomic neuropathy with deafness and global delayG60.8Hermansky-Pudlak syndrome type 8E70.3Hirschsprung diseaseQ43.1Hirschsprung disease-nail hypoplasia-dysmorphism syndromeQ87.8HSPB8-related autosomal dominant distal axonal motor neuropathy-myofibrillar myopathy syndromeG60.3Human infection by orthopoxvirusB08.0Huriez syndromeQ82.8Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiencyD68.59Hyperlipidemia due to hepatic triacylglycerol lipase deficiencyE78.5Hypomyelination with atrophy of basal ganglia and cerebellumG37.8