Pages that link to "Property:P78"
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The following pages link to Knowledge Architect (P78):
Displaying 50 items.
- Congenital scoliosis due to congenital bony malformation (Q46590) (← links)
- Cervical rib (Q46591) (← links)
- Structural developmental anomalies of sternum (Q46592) (← links)
- Achondrogenesis (Q46593) (← links)
- Hypochondrogenesis (Q46594) (← links)
- Thanatophoric dysplasia (Q46595) (← links)
- Short rib-polydactyly syndrome (Q46596) (← links)
- Short rib syndromes (Q46597) (← links)
- Asphyxiating thoracic dystrophy (Q46598) (← links)
- Chondrodysplasia punctata (Q46599) (← links)
- Hypochondroplasia (Q46600) (← links)
- Achondroplasia (Q46601) (← links)
- Diastrophic dysplasia (Q46602) (← links)
- Spondylometaphyseal dysplasias (Q46603) (← links)
- Spondylodysplastic dysplasias (Q46604) (← links)
- Osteogenesis imperfecta (Q46605) (← links)
- Osteopetrosis (Q46606) (← links)
- Multiple metaphyseal dysplasias (Q46607) (← links)
- Multiple osteochondromas (Q46608) (← links)
- Osteopoikilosis (Q46609) (← links)
- Bone diseases with increased bone density (Q46610) (← links)
- Congenital diaphragmatic hernia (Q46611) (← links)
- Absence of diaphragm (Q46612) (← links)
- Omphalocele (Q46613) (← links)
- Gastroschisis (Q46614) (← links)
- Prune belly syndrome (Q46615) (← links)
- Ehlers-Danlos syndrome, classical type (Q46616) (← links)
- Ehlers-Danlos syndrome (Q46617) (← links)
- Genetic bone diseases with decreased bone density (Q46618) (← links)
- Bone dysplasias with multiple joint dislocations (Q46619) (← links)
- Langer-Giedion syndrome (Q46620) (← links)
- Acromesomelic dysplasias (Q46621) (← links)
- Slender bone dysplasias (Q46622) (← links)
- Pseudoachondroplasia (Q46623) (← links)
- Bent bone dysplasias (Q46624) (← links)
- Acromelic dysplasias (Q46625) (← links)
- Multiple epiphyseal dysplasias (Q46626) (← links)
- Mesomelic or rhizomesomelic dysplasias (Q46627) (← links)
- Bone diseases with disorganised development of skeletal components (Q46628) (← links)
- Progressive ossification of skin, skeletal muscle, fascia, tendons or ligaments (Q46629) (← links)
- Dysostoses with predominant vertebral and costal involvement (Q46630) (← links)
- Multiple epiphyseal dysplasia or pseudoachondroplasia (Q46631) (← links)
- Apert syndrome (Q46632) (← links)
- Structural developmental anomalies of diaphragm (Q46633) (← links)
- Syndromic ichthyosis (Q46634) (← links)
- Ichthyosis vulgaris (Q46635) (← links)
- X-linked ichthyosis (Q46636) (← links)
- Junctional epidermolysis bullosa (Q46637) (← links)
- Epidermolysis bullosa simplex (Q46638) (← links)
- Dystrophic epidermolysis bullosa (Q46639) (← links)
