hereditary disease
MONDO:0003847Mondo
Findings
No curated finding names hereditary disease yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome.
Definition from the Mondo Disease Ontology (MONDO:0003847), read 2026-09-29. CC BY 4.0.
Where it sits
- Narrower terms (1,921)
- Achard syndrome
- Achoo syndrome
- acroleukopathy, symmetric
- acromegaloid changes, cutis verticis gyrata, and corneal leukoma
- acromial dimples
- Adams-Oliver syndrome
- adenosine triphosphatase deficiency, anemia due to
- alopecia-epilepsy-pyorrhea-intellectual disability syndrome
- amastia, bilateral, with ureteral triplication and dysmorphism
- amelia and terminal transverse hemimelia
- anemia, hypochromic microcytic with iron overload
- ariboflavinosis
- autoimmune disease, multisystem, infantile-onset
- autosomal genetic disease
- bone marrow failure syndrome
- bone Paget disease
- bronchiectasis
- camptodactyly syndrome, Guadalajara
- cataract
- celiac disease
- cerebelloparenchymal disorder
- Chiari malformation
- ciliopathy
- congenital diarrhea
- cornea plana
- developmental dysplasia of the hip
- epithelial-stromal TGFBI dystrophy
- familial abdominal aortic aneurysm
- familial hemolytic anemia
- familial polycythemia
- febrile seizures, familial
- FG syndrome
- fibromuscular dysplasia
- Fuchs' endothelial dystrophy
- hereditary fallopian tube carcinoma
- hereditary hypophosphatemic rickets
- hereditary Wilms tumor
- hydatidiform mole
- hypospadias
- hypothyroidism, congenital, nongoitrous
- hypotrichosis
- infantile liver failure
- inflammatory bowel disease
- inherited aplastic anemia
- inherited bleeding disorder, platelet-type
- isolated microphthalmia
- Klippel-Feil syndrome
- multinodular goiter
- myopia
- nanophthalmia
- nephrolithiasis/osteoporosis, hypophosphatemic
- orofacial cleft
- preeclampsia
- spermatogenic failure
- spondylocostal dysostosis
- tooth agenesis
- visceral leishmaniasis
- X-linked disease
- Y-linked disease
- Zimmermann-Laband syndrome
- and 1,861 more
Other names
5 names
Resolves to: hereditary disease
- Also called
- hereditary disease or disorderhereditary diseasesinherited diseaseinherited genetic diseasemolecular disease