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Eligible Country
Eye Color
Hair Type
Natural Hair Color
Complexion
Religion
Ancestry
Blood Type
CMV Status
Vial Types
Genetic Testing
Each of our donors are tested for an extensive list of genetic conditions. Find conditions donors are negative for.
- 17-Beta Hydroxysteroid Dehydrogenase 3 Deficiency (HSD17B3)
- 2-Methyl-3-Hydroxybutyric Aciduria X-Linked (HSD17B10)
- 21-Alpha-Hydroxylase-Deficient Congenital Adrenal Hyperplasia (CYP21A2)
- 3-Hydroxy-3-Methylglutaryl-CoA (HMG-CoA) Lyase Deficiency (HMGCL)
- 3-Methylcrotonyl-CoA Carboxylase Deficiency MCCC1-Related (MCCC1)
- 3-Methylcrotonyl-CoA Carboxylase Deficiency MCCC2-Related (MCCC2)
- 3-Methylglutaconic Aciduria Type III also known as Costeff Optic Atrophy (OPA3)
- 3-Phosphoglycerate Dehydrogenase Deficiency PHGDH-Related (PHGDH)
- 6-Pyruvoyl-Tetrahydropterin Synthase Deficiency (PTS)
- ABCA3-Related Disorders (ABCA3)
- ABCA4-Related Disorders (ABCA4)
- ABCC6-Related Disorders (ABCC6)
- ABCD4-Related Disorders (ABCD4)
- Abetalipoproteinemia (MTTP)
- ACADSB-Related Disorders (ACADSB)
- Achromatopsia (CNGB3)
- Achromatopsia 2 (CNGA3)
- Acrodermatitis Enteropathica (SLC39A4)
- Acute Infantile Liver Failure (TRMU)
- Acyl-CoA Oxidase I Deficiency (ACOX1)
- Adams-Oliver Syndrome 4 (EOGT)
- Adenosine Deaminase 2 Deficiency (ADA2)
- Adenosine Deaminase Deficiency (ADA)
- ADGRV1-Related Disorders (ADGRV1)
- Adrenoleukodystrophy, X-Linked (ABCD1)
- Agammaglobulinemia X-Linked (BTK)
- AGPAT2-Related Disorders (AGPAT2)
- AHI1-Related Disorders (AHI1)
- Aicardi-Goutieres Syndrome (SAMHD1)
- Aicardi-Goutieres Syndrome 2 (RNASEH2B)
- Aicardi-Goutieres Syndrome 3 (RNASEH2C)
- Aicardi-Goutieres Syndrome 4 (RNASEH2A)
- AICDA-Related Disorders (AICDA)
- AK2-Related Disorders (AK2)
- Aldosterone Synthase Deficiency also known as Corticosterone Methyloxidase Deficiency (CYP11B2)
- ALG13-Related Disorders X-Linked (ALG13)
- Alkaptonuria (HGD)
- ALOX12B-Related Disorders (ALOX12B)
- ALOXE3-Related Disorders (ALOXE3)
- Alpha-1 Antitrypsin Deficiency (SERPINA1)
- Alpha-Mannosidosis (MAN2B1)
- Alpha-N-Acetylgalactosaminidase Deficiency (NAGA)
- Alpha-Thalassemia (HBA1/HBA2)
- Alpha-Thalassemia Intellectual Disability Syndrome X-Linked (ATRX)
- Alport Syndrome, COL4A3-Related (COL4A3)
- Autosomal recessive congenital myotonia
- Cystinosis
- Oculocutaneous albinism type lI
- PMM2- glycosylation disorders (PMM2)
- Pompe disease (GAA)
- Primary ciliary dyskinesia DNAH5-related
- Short-chain acyl-coA dehydrogenase (SCAD) deficiency
- Smith-Lemli-Opitz syndrome (DHCR7)
- Systemic primary carnitine deficiency
- Trimethylaminuria (FMO3)
- Triple A Syndrome (AAAS)
- TSEN2-Related Disorders (TSEN2)
- TSEN34-Related Disorders (TSEN34)
- TSHR-Related Disorders (TSHR)
- TTC7A-Related Disorders (TTC7A)
- TTC8-Related Disorders (TTC8)
- TULP1-Related Disorders (TULP1)
- Tyrosine Hydroxylase Deficiency (TH)
- Tyrosinemia Type 1 (FAH)
- Tyrosinemia Type III (HPD)
- Tyrosinemia, Type II (TAT)
- UNG-Related Disorders (UNG)
- USH1G-Related Disorders (USH1G)
- Usher Syndrome Type 2C and AGDRV1-Related Disorders (AGDRV1)
- Usher Syndrome Type IB (MYO7A)
- Usher Syndrome Type IC (USH1C)
- Usher Syndrome Type ID (CDH23)
- Usher Syndrome Type IF (PCDH15)
- Usher Syndrome Type IIA (USH2A)
- Usher Syndrome Type IIIA (CLRN1)
- Vanishing White Matter Disease (EIF2B5)
- Very Long Chain Acyl-CoA Dehydrogenase Deficiency (ACADVL)
- Very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency
- Vici Syndrome (EPG5)
- Vitamin D-Dependent Rickets Type 1A (CYP27B1)
- Vitamin D-Dependent Rickets Type 2A (VDR)
- VPS53-Related Disorders (VPS53)
- Warsaw Syndrome (DDX11)
- WAS-Related Disorders X-Linked (WAS)
- Werner Syndrome (WRN)
- WHRN-Related Disorders (WHRN)
- Wilson Disease (ATP7B)
- WNT1-Related Disorders (WNT1)
- Wolcott-Rallison Syndrome (EIF2AK3)
- Woodhouse-Sakati Syndrome (DCAF17)
- Xeroderma Pigmentosum Group A (XPA)
- Xeroderma Pigmentosum Group C (XPC)
- Xeroderma Pigmentosum Variant Type (POLH)
- ZAP70-Related Disorders (ZAP70)
- Zellweger Spectrum Disorder PEX1-Related (PEX1)
- Zellweger Spectrum Disorder PEX13-Related (PEX13)
- Zellweger Spectrum Disorder PEX16-Related (PEX16)
- Zellweger Spectrum Disorder PEX2-Related (PEX2)
- Zellweger Spectrum Disorder PEX26-Related (PEX26)
- Zellweger Spectrum Disorder, PEX6-Related (PEX6)
- Zellweger Syndrome Spectrum (PEX1)
- Zellweger Syndrome Spectrum PEX10- Related (PEX10)
Filter out donors that have tested positive for chosen genetic conditions. If a condition does not appear on this list, our donors have not tested positive for it. For a complete list of conditions screened, please contact us, or view the full gene panel PDF included on each donor profile.
Advanced Options
Height
Weight
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Austin, #0005
0Cryomate Success: This number indicates the amount of proven families that have been conceived with this donor.6’3” | 185 lbs-
Hair Color: Medium Blond
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Eye Color: Blue
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Ancestry: Caucasian
There are 11–25 vials for this donor available.Open ID: This donor is open to future contact with donation-born offspring over the age of 18.The donor is compliant for purchase in the U.K.The donor is compliant for purchase in Israel. -
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Gabe, #0006
0Cryomate Success: This number indicates the amount of proven families that have been conceived with this donor.5’10” | 210 lbs-
Hair Color: Black
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Eye Color: Brown
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Ancestry: Caucasian, Mexican
There are 11–25 vials for this donor available.Fertility Potential: This donor has children of their own.Open ID: This donor is open to future contact with donation-born offspring over the age of 18.The donor is compliant for purchase in the U.S.A.The donor is compliant for purchase in the U.K.The donor is compliant for purchase in Israel. -
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Joshua, #0001
0Cryomate Success: This number indicates the amount of proven families that have been conceived with this donor.6’3” | 245 lbs-
Hair Color: Medium Blond
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Eye Color: Green
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Ancestry: Caucasian, Native American
There are more than 25 vials for this donor available.Fertility Potential: This donor has children of their own.Open ID: This donor is open to future contact with donation-born offspring over the age of 18.The donor is compliant for purchase in the U.S.A.The donor is compliant for purchase in the U.K.The donor is compliant for purchase in Israel. -
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Matthew, #0002
0Cryomate Success: This number indicates the amount of proven families that have been conceived with this donor.6’2” | 200 lbs-
Hair Color: Medium Blond
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Eye Color: Hazel
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Ancestry: Caucasian, Native American
There are 11–25 vials for this donor available.Fertility Potential: This donor has children of their own.Open ID: This donor is open to future contact with donation-born offspring over the age of 18.The donor is compliant for purchase in the U.S.A.The donor is compliant for purchase in the U.K.The donor is compliant for purchase in Israel. -
ICON DICTIONARY
ICON DICTIONARY
Vials & Donor Status
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There are more than 25 vials for this donor available.
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There are 11–25 vials for this donor available.
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There are less than 10 vials for this donor available.
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Fertility Potential: This donor has children of their own.
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Anonymous ID: This donor does not wish to release identity.
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Open ID: This donor is open to future contact with donation-born offspring over the age of 18.
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Cryomate Success: This number indicates the amount of proven families that have been conceived with this donor.
Shipping Compliancy
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The donor is compliant for purchase in the U.S.A.
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The donor is compliant for purchase in the U.K.
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The donor is compliant for purchase in Europe
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The donor is compliant for purchase in Canada
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The donor is compliant for purchase in the Australia.
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The donor is compliant for purchase in Israel.