Experimental Factor Ontology
692 terms(s) returned
Term Type: | Record: 451 to 500 of 692 Records | Page: 10 of 14, First Previous Next Last | Show Records Per Page |
- hyaline fibromatosis syndrome
- hydatidiform mole, recurrent, 1
- hydranencephaly
- hydrarthrosis
- hydrocephalus, congenital, 3, with brain anomalies
- hydrocephalus, congenital, 5, susceptibility to
- hydrocephalus-blue sclerae-nephropathy syndrome
- hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome
- hydrocephalus-obesity-hypogonadism syndrome
- hydrocephaly-cerebellar agenesis syndrome
- hydrocephaly-tall stature-joint laxity syndrome
- hydrolethalus syndrome
- hydrolethalus syndrome 2
- hydrops fetalis
- hydrops-lactic acidosis-sideroblastic anemia-multisystemic failure syndrome
- hydroxyprolinemia
- hyper-IgE recurrent infection syndrome 1, autosomal dominant
- hyper-IgE recurrent infection syndrome 4A, autosomal dominant
- hyper-IgE recurrent infection syndrome 5, autosomal recessive
- hyper-IgE syndrome
- hyper-IgE syndrome 6, autosomal dominant, with recurrent infections
- hyper-IgM syndrome
- hyper-IgM syndrome type 1
- hyper-IgM syndrome type 2
- hyper-IgM syndrome type 3
- hyper-IgM syndrome type 4
- hyper-IgM syndrome type 5
- hyper-beta-alaninemia
- hyperalphalipoproteinemia
- hyperammonemia due to N-acetylglutamate synthase deficiency
- hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency
- hyperargininemia
- hyperbiliverdinemia
- hypercalcemia disease
- hypercalcemia, infantile
- hypercalcemia, infantile, 2
- hypercalcemic sarcoidosis
- hypercholanemia, familial
- hypercholanemia, familial 1
- hypercholanemia, familial, 2
- hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency
- hypercholesterolemia, autosomal dominant, 3
- hypercholesterolemia, autosomal dominant, type B
- hypercholesterolemia, familial, 1
- hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
- hyperdibasic aminoaciduria type 1
- hyperekplexia
- hyperemesis gravidarum, susceptibility to
- hypergonadotropic hypogonadism-cataract syndrome
- hyperhomocysteinemia