Health analysis for Doux Berger Magic Star

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.

	Date of birth	Year of death	Canine Multifocal Retinopathy 3 (CMR3)	Degenerative myelopathy (DM)	Elbows	Glycogen storage disease type II (Pompe disease) (GSDII)	Hips	Progressive retinal atrophy (prcd-PRA)
Parents
Jarfa's Kratti	7 Aug 2017	0 (null yrs)			normal	N/N (clear)	Good / A2 / 1-3 / A / 5-10 (no >6/hip)	N/N (clear)
Elbows: normal Glycogen storage disease type II (Pompe disease) (GSDII): N/N (clear) Hips: Good / A2 / 1-3 / A / 5-10 (no >6/hip) Progressive retinal atrophy (prcd-PRA): N/N (clear)
Miss Fiona du Doux Berger	26 Jul 2018	0 (null yrs)			normal	N/N (clear)	Good / A2 / 1-3 / A / 5-10 (no >6/hip)
Elbows: normal Glycogen storage disease type II (Pompe disease) (GSDII): N/N (clear) Hips: Good / A2 / 1-3 / A / 5-10 (no >6/hip)
Siblings
Half siblings (sire)
Doux Berger Shinto du Soleil	23 Dec 2019	0 (null yrs)
Doux Berger Shiny Flower	18 Feb 2021	0 (null yrs)
Doux Berger Salmiakki	31 Jul 2022	0 (null yrs)
MapleMyst Gobi-Wan-Kenobe	8 May 2024	0 (null yrs)
MapleMyst Holding Out for a Hero	8 May 2024	0 (null yrs)
MapleMyst Jedi Knight Hero of the Galaxy	8 May 2024	0 (null yrs)
MapleMyst The Princess Knight	8 May 2024	0 (null yrs)
MapleMyst We All Are Heroes	8 May 2024	0 (null yrs)
MapleMyst's Calling the Shots	8 May 2024	0 (null yrs)
MapleMyst's Hiro Sankari	8 May 2024	0 (null yrs)
MapleMyst's Kibeth the Walker	8 May 2024	0 (null yrs)
Half siblings (dam)
DouxBerger Winter Nights	10 Dec 2022	0 (null yrs)
Offspring
Lighthouse Snowbelle	31 Jan 2023	0 (null yrs)
Lighthouse Mikko	27 Apr 2023	0 (null yrs)
Lighthouse Wilco Over and Out	15 Nov 2023	0 (null yrs)	N/N (clear)	N/N (clear)		N/N (clear)		N/mut (carrier)
Canine Multifocal Retinopathy 3 (CMR3): N/N (clear) Degenerative myelopathy (DM): N/N (clear) Glycogen storage disease type II (Pompe disease) (GSDII): N/N (clear) Progressive retinal atrophy (prcd-PRA): N/mut (carrier)