Mondo Disease Ontology
2507 terms(s) returned
| Term Type: | Record: 1251 to 1300 of 2507 Records | Page: 26 of 51, First Previous Next Last | Show Records Per Page |
- hereditary angioedema with C1Inh deficiency
- hereditary angioedema with normal C1Inh
- hereditary angioedema with normal C1inh not related to F12 or PLG variant
- hereditary anorectal anomalies
- hereditary antithrombin deficiency
- hereditary arterial and articular multiple calcification syndrome
- hereditary ataxia
- hereditary ataxia, non-human animal
- hereditary attention deficit-hyperactivity disorder
- hereditary benign intraepithelial dyskeratosis
- hereditary breast carcinoma
- hereditary breast ovarian cancer syndrome
- hereditary cerebellar ataxia
- hereditary cerebellar ataxia, KCNIP4-related, dog
- hereditary cerebellar ataxia, non-human animal
- hereditary cerebral malformation
- hereditary chondrodysplasia, dog
- hereditary choroidal atrophy
- hereditary chronic pancreatitis
- hereditary clear cell renal cell carcinoma
- hereditary continuous muscle fiber activity
- hereditary coproporphyria
- hereditary cryohydrocytosis with reduced stomatin
- hereditary dementia
- hereditary diffuse gastric adenocarcinoma
- hereditary disease
- hereditary disease, non-human animal
- hereditary disorder of connective tissue
- hereditary elliptocytosis
- hereditary endocrine growth disease
- hereditary epidermal appendage anomaly
- hereditary episodic ataxia
- hereditary fallopian tube carcinoma
- hereditary folate malabsorption
- hereditary footpad hyperkeratosis, FAM83G-related, dog
- hereditary fructose intolerance
- hereditary gallbladder disorder
- hereditary gastric cancer
- hereditary generalized epilepsy
- hereditary geniospasm
- hereditary gingival fibromatosis
- hereditary glaucoma
- hereditary glaucoma, primary closed-angle
- hereditary hemochromatosis
- hereditary hemolytic uremic syndrome
- hereditary hemophagocytic lymphohistiocytosis
- hereditary hemorrhagic telangiectasia
- hereditary hemorrhagic telangiectasia type 3
- hereditary hemorrhagic telangiectasia type 4
- hereditary hyperbilirubinemia