Pages that link to "WikibaseProperty:P1199"
The following pages link to mode of inheritance (P1199):
Displayed 30 items.
- phenotypic trait (Q1211967) (← links)
- mode of inheritance (Q1348351) (← links)
- hemophilia C (Q1393718) (← links)
- facioscapulohumeral muscular dystrophy (Q1399182) (← links)
- Bloom syndrome (Q1469646) (← links)
- porphyria cutanea tarda (Q1479497) (← links)
- mucopolysaccharidosis II (Q1529983) (← links)
- Sanfilippo syndrome (Q2200359) (← links)
- Sly syndrome (Q1750471) (← links)
- congenital erythropoietic porphyria (Q1759389) (← links)
- erythropoietic protoporphyria (Q1759600) (← links)
- Job's syndrome (Q2336873) (← links)
- mucopolysaccharidosis I (Q1906054) (← links)
- Alpers' disease (Q2028015) (← links)
- hemophilia B (Q2562598) (← links)
- hemophilia A (Q2092064) (← links)
- chromosome 1q21.1 duplication syndrome (Q2692054) (← links)
- autosomal dominant polycystic kidney (Q2732398) (← links)
- autosomal recessive polycystic kidney (Q3395618) (← links)
- mevalonic aciduria (Q3043158) (← links)
- Flynn–Aird syndrome (Q5463653) (← links)
- mucopolysaccharidosis IX (Q5473408) (← links)
- GRACILE syndrome (Q5514398) (← links)
- recessive dystrophic epidermolysis bullosa (Q7302398) (← links)
- Spider lamb syndrome (Q7577061) (← links)
- neurofibromatosis type I (Q7616509) (← links)
- Vohwinkel syndrome (Q7939442) (← links)
- Bartsocas-Papas syndrome (Q9390213) (← links)
- autosomal recessive disease (Q10267817) (← links)
- mode of inheritance (P1199) (← links)