Health analysis for Niloksen Mysti

Generations:

Please note: If no health information is shown for an animal, this does not necessarily mean that the animal is healthy but merely that no information was provided.

Niloksen Mysti 2018, COI 0.75 % *	Murustiinan Erityisen Ihana FIN 2013, COI 2.32 % *	Murustiinan Valkorinta FIN 2010, COI 1.25 % * Year of death: 2023 Cause of death: Old age (unspecified cause of death) -	Levi FIN 2007, COI 2.38 % *
			Fidelis Gorassu FIN 2008, COI 2.55 %
		Murustiinan Bella FIN 2009, COI 1.55 % *	Garmelin Iltavalo FIN 2000, COI 3.04 % *
		Murustiinan Bella FIN 2009, COI 1.55 % *	Riide FIN 2007, COI 6.21 % *
	Yestas Yessi FIN 2015, COI 3.24 % *	Pörröpöksyn Koti-Kontio FIN 2010, COI 1.17 % *	Orso-Farm Kiusa FIN 2002, COI 2.98 % * Breed relevant health information: Hips Excellent / A1 / 0 / A / 0-4 (no >3/hip) - Year of death: 2015 Cause of death: Euthanasia (unspecified reason) -
		Pörröpöksyn Koti-Kontio FIN 2010, COI 1.17 % *	Fihtolas Yopo FIN 2006, COI 0.89 % * Breed relevant health information: Elbows normal - Glycogen storage disease type II (Pompe disease) (GSDII) N/N (clear) - Hips Excellent / A1 / 0 / A / 0-4 (no >3/hip) - Progressive retinal atrophy (prcd-PRA) N/N (clear) - Year of death: 2021 Cause of death: Old age (unspecified cause of death) -
		Eisenfest Taivas Varjele FIN 2011, COI 3.82 %	Lapinpeikon Häntä Heikki FIN 2007, COI 5.76 % *
		Eisenfest Taivas Varjele FIN 2011, COI 3.82 %	Lumiturpa Oikun Hilla FIN 2005, COI 1.86 % Breed relevant health information: Elbows normal - 22/9/2011 Hips Good / A2 / 1-3 / A / 5-10 (no >6/hip) - 22/9/2006 Year of death: 2017

* COI cannot be reliably calculated due to incomplete generations in the pedigree!

Pedigree generated by breedarchive.com at 28/3/2025

The information on this page shows a snap-shot of the relevant data available in The Breed Archive at the time the page was created, with no guarantee with regard to the completeness or correctness of the data (the data having been provided by the user community). The Breed Archive accepts no liability with respect to the information shown or any conclusions drawn from it.

	Date of birth	Year of death	Degenerative myelopathy (DM)	Elbows	Glycogen storage disease type II (Pompe disease) (GSDII)	Hips	Progressive retinal atrophy (prcd-PRA)
Parents
Murustiinan Erityisen Ihana	1 May 2013	0 (null yrs)
Yestas Yessi	9 Apr 2015	0 (null yrs)
Siblings
Niloksen Maisi	25 Mar 2018	0 (null yrs)
Niloksen Malina	25 Mar 2018	0 (null yrs)
Niloksen Manta	25 Mar 2018	0 (null yrs)
Niloksen Möykky	25 Mar 2018	0 (null yrs)
Niloksen Mutru	25 Mar 2018	0 (null yrs)
Niloksen Muumi	25 Mar 2018	0 (null yrs)
Half siblings (sire)
Pakkaspöksyn Caunis Camomilla	29 Nov 2017	0 (null yrs)
Pakkaspöksyn Cicattava Carpalo	29 Nov 2017	0 (null yrs)
Pakkaspöksyn Ciehtova Castanja	29 Nov 2017	0 (null yrs)
Pakkaspöksyn Cujeileva Couscous	29 Nov 2017	0 (null yrs)				Good / A2 / 1-3 / A / 5-10 (no >6/hip)
Hips: Good / A2 / 1-3 / A / 5-10 (no >6/hip)
Pakkaspöksyn Cuuma Caacao	29 Nov 2017	0 (null yrs)
Niloksen Mustamaija	24 May 2018	0 (null yrs)
Niloksen Mustamarja	24 May 2018	0 (null yrs)
Niloksen Parkkipate	24 May 2018	0 (null yrs)
Niloksen Parkkiperhonen	24 May 2018	0 (null yrs)
Niloksen Parkkipete	24 May 2018	0 (null yrs)
Niloksen Parkkipilvi	24 May 2018	0 (null yrs)
Niloksen Parkkipimu	24 May 2018	0 (null yrs)
Niloksen Parkkipirkko	24 May 2018	0 (null yrs)
Half siblings (dam)
Expected Americano	29 Mar 2017	0 (null yrs)
Expected Cappuccino	29 Mar 2017	0 (null yrs)
Expected Corretto	29 Mar 2017	0 (null yrs)
Expected Cortado	29 Mar 2017	0 (null yrs)
Expected Espresso	29 Mar 2017	0 (null yrs)
Expected Frappuccino	29 Mar 2017	0 (null yrs)
Expected Macciato	29 Mar 2017	0 (null yrs)
Expected Mochalatte	29 Mar 2017	0 (null yrs)
Niloksen Pinocchio	4 Jan 2020	0 (null yrs)
Niloksen Pocahontas	4 Jan 2020	0 (null yrs)
Niloksen Ruusunen	4 Jan 2020	0 (null yrs)
Niloksen Tuhkimo	4 Jan 2020	0 (null yrs)	N/mut (carrier)	normal	N/N (clear)	Fair / B1 / 4-6 / B / 11-18	N/mut (carrier)
Degenerative myelopathy (DM): N/mut (carrier) Elbows: normal Glycogen storage disease type II (Pompe disease) (GSDII): N/N (clear) Hips: Fair / B1 / 4-6 / B / 11-18 Progressive retinal atrophy (prcd-PRA): N/mut (carrier)
Offspring