People with dwarfism and conditions of short stature. Achondrogenesis; Achondroplasia; Acrodysostosis; Acromesomelic Dysplasia; Acromesomelic Dysplasia Maroteaux Type; AMDM;
Atelosteogenesis; Campomelic Dysplasia;
Cartilage Hair Hypoplasia; CHH; Metaphyseal; Chondrodysplasia; McKusick type; Chondrodysplasia Punctata;
Cleidocranial Dysostosis; Conradi-Hunermann; Syndrome; Cornelia de Lange; Cranioectodermal dysplasia; Desbuquois syndrome; Diastrophic Dysplasia; Dyggve-Melchior-Clausen; Dyssegmental Dysplasia; Ellis van Creveld Syndrome; Chondroectodermal Dysplasia EVC; Growth Hormone Deficiency; Hallerman-Streiff Syndrome; Hunter Syndrome; MPS II; Hurler-Scheie Syndrome; MPS I; Hypochondrogenesis; Hypochondroplasia; Hypophosphatasia; Hypophosphatemia; Hypopituitary; Hypothyroidism; Jarcho-Levin Syndrome Spondylothoracic Dysplasia Spondylocostal; Jeune Syndrome Asphyxiating Thoracic Dysplasia; Asphyxiating Thoracic Dystrophy; Kniest Dysplasia; Laron Dwarfism; Larsen Syndrome; Leri-Weill Dyschondrosteosis Mesomelic Dwarfism, Madelung Deformity; Lethal Skeletal Dysplasias; Maroteaux-Lamy MPS VI MPS VI; Mesomelic Dysplasia; Metaphyseal Chondrodysplasia-Jansen Type; Metaphyseal Dysplasia-Schmid Type; Metatropic Dysplasia; Morquio Syndrome MPS IV; Mucopolysaccharidoses; Multiple Epiphyseal Dysplasia MED; Osteogenesis Imperfecta OI; Pituitary Dwarfism; Precocious Puberty; Primordial; Dwarfism; Microcephalic Osteodysplastic; Primordial Dwarfism MOPD; Pseudoachondroplasia
Rhizomelic Chondrodysplasia Punctata; Rickets
Robinow dwarfism syndrome; Russell-Silver Syndrome; SADDAN: Severe Achondroplasia with Acanthosis Nigricans and Developmental Delay; Schmike Immuneosseous Dysplasia; Seckel Syndrome; Short Rib Polydactyly; Shwachman-Diamond Syndrome; Spondyloepimetaphyseal Dysplasia-Strudwick SEMD; Spondyloepimetaphyseal dysplasias; Spondyloepiphyseal Dysplasia; Spondyloepiphyseal Dysplasia Congenita SED-Congenita SEDC;
Spondyloepiphyseal Dysplasia Tarda SED-Tarda SEDT SED-L;
Spondylometaphyseal Dysplasia-Corner Fracture Type SMD SMD-Corner Fracture Type SMD-Sutcliffe Type; Spondylometaphyseal Dysplasia-Kozlowski SMD-Kozlowski SMDK; Thanatophoric Dysplasia
Trichorhinophalangeal Syndrome (Langer-Giedion syndrome)
Turner Syndrome
Type II Collagenopathies

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Little People of New Zealand (LPNZ)

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Our Collective

Rare Disorders NZ is the collective voice of all people living with a rare disorder and their whānau. Our rare collective is made up of more than 160 disorder-specific support groups.

Our work is informed by the issues important to our collective. We work together to improve healthcare and wellbeing for everyone living with a rare health condition in New Zealand.

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