Nā ʻetlelo Genetics / Hānau Hānau
Mea Kākau:
Joan Hall
Lā O Ka Hana:
25 Pepeluali 2021
HōʻAno Hou I Ka Lā:
4 Apelila 2025
- Nā mea kūpono ʻole ʻike Hewa hānau
- Achondroplasia ʻike ʻO Dwarfism
- Adrenoleukodystrophy ʻike Nā Leukodystrophies
- Ka nele o Alpha-1 Antitrypsin
- ʻO Amniocentesis ʻike Hōʻikeʻike Prenatal
- Anencephaly ʻike Nā hemahema Tube Neural
- ʻO Maloldation ʻo Arnold-Chiari ʻike ʻO Chiari Malformation
- Ataxia ʻike Friedreich Ataxia
- Ataxia Telangiectasia
- Hewa hānau
- Nā maʻi hōʻeha koko ʻike Hemopilia
- Nā maʻi o ka lolo, Genetic Inborn ʻike Nā maʻi Brain Genetic
- Malformations o ka lolo
- ʻO ka maʻi Canavan ʻike Nā Leukodystrophies
- Nā maʻi Cephalic ʻike Malformations o ka lolo
- ʻO Cerebral Palsy
- ʻO ka maʻi ʻo Charcot-Marie-Tooth
- ʻO Chiari Malformation
- ʻO Chorionic Villi Laʻana ʻike Hōʻikeʻike Prenatal
- Lip Lip a me Palate
- Pālolo Maʻa ʻike Lip Lip a me Palate
- Spine Spine ʻike ʻO Spina Bifida
- Kalaunu
- Ka makapō makapō
- Nā Puʻuwai Puʻuwai Congenital
- ʻO ka maʻi mālama keleawe ʻike Maʻi ʻo Wilson
- Nā pono ʻole Craniofacial
- Craniosynostosis ʻike Nā pono ʻole Craniofacial
- ʻO Cystic Fibrosis
- Down Syndrome
- ʻO Duchenne Muscular Dystrophy ʻike Muscular Dystrophy
- ʻO Dwarfism
- Ehlers-Danlos Syndrome
- Mōʻaukala ʻohana
- ʻO FAS ʻike Nā maʻi Spectrum Alkohol Fetal
- Nā maʻi Spectrum Alkohol Fetal
- Fetal Alcohol Syndrome ʻike Nā maʻi Spectrum Alkohol Fetal
- Fetal Ultrasound ʻike Hōʻikeʻike Prenatal
- Fragile X Syndrome
- FRAXA ʻike Fragile X Syndrome
- Friedreich Ataxia
- Hema G6PD
- ʻO ka maʻi Gaucher
- ʻO Genes a me Gene Therapy
- Nā maʻi Brain Genetic
- ʻSellelo aʻoaʻo genetic
- Nā maʻi genetic
- Hōʻike genetic
- ʻO ka Glucose-6-phosphate Dehydrogenase Deficience ʻike Hema G6PD
- Nā Puʻuwai Puʻuwai ʻike Nā Puʻuwai Puʻuwai Congenital
- Nā maʻi puʻuwai, hānau hānau ʻike Nā Puʻuwai Puʻuwai Congenital
- ʻŌhumu puʻuwai ʻike Nā Puʻuwai Puʻuwai Congenital
- Hemochromatosis
- ʻO ka maʻi Hemoglobin SS ʻike ʻO ka maʻi maʻi maʻi maʻi
- Hemopilia
- Hepatolenticular Degeneration ʻike Maʻi ʻo Wilson
- Pāhana Genome Kānāwai ʻike ʻO Genes a me Gene Therapy
- ʻO ka maʻi ʻo Huntington
- ʻO Hydrocephalus
- Hypermobility Syndrome ʻike Ehlers-Danlos Syndrome
- ʻO ka maʻi ʻoi loa ka hao ʻike Hemochromatosis
- ʻO Klinefelter Syndrome
- Nā Leukodystrophies
- ʻO ka maʻi mimi Maple Syrup ʻike Nā maʻi Brain Genetic
- ʻO Marfan Syndrome
- Nā Lapaʻau a me ka Hapai ʻike Hāpai a me nā Lapaʻau
- Nā maʻi Metabolic
- ʻO Mucolipidoses ʻike Nā maʻi Metabolic
- Muscular Dystrophy
- Myelomeningocele ʻike ʻO Spina Bifida
- Nā hemahema Tube Neural
- Neurofibromatosis
- Nānā Hou
- ʻO ka maʻi Niemann-pick ʻike Nā maʻi Brain Genetic
- Wehewehe i ka iwi kuamoʻo ʻike ʻO Spina Bifida
- ʻO Osteogenesis Imperfecta
- Hōʻoiaʻiʻo Paternity ʻike Hōʻike genetic
- Phenylketonuria
- PKU ʻike Phenylketonuria
- Plagiocephaly Position ʻike Nā pono ʻole Craniofacial
- ʻO Prader-Willi Syndrome
- Hāpai a me nā Lapaʻau
- Hōʻikeʻike Prenatal
- Progeria ʻike Nā maʻi genetic
- Nā maʻi kakaikahi
- Ret Syndrome
- Nānā ʻia, Hānau Hou ʻike Nānā Hou
- Anemia Sickle Cell ʻike ʻO ka maʻi maʻi maʻi maʻi
- ʻO ka maʻi maʻi maʻi maʻi
- SMA ʻike Spinal Muscular Atrophy
- ʻO Spina Bifida
- Spinal Muscular Atrophy
- ʻO ka maʻi ʻo Tay-Sachs
- Tourette Syndrome
- ʻO Treacher-Collins Syndrome ʻike Nā pono ʻole Craniofacial
- ʻO Trisomy 21 ʻike Down Syndrome
- TSC ʻike ʻO Tuberous Sclerosis
- ʻO Tuberous Sclerosis
- ʻO Turner Syndrome
- Usher Syndrome
- VHL ʻike ʻO ka maʻi ʻo Von Hippel-Lindau
- ʻO ka maʻi ʻo Von Hippel-Lindau
- ʻO ka maʻi ʻo Recklinghausen ʻike Neurofibromatosis
- Maʻi ʻo Wilson
ʻO Kā Mākou’Ōlelo
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