Pages that link to "Property:P68"
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The following pages link to Canonical URI (P68):
Displaying 50 items.
- Congenital contractural arachnodactyly (Q46716) (← links)
- Marfan syndrome (Q46717) (← links)
- Exostoses with anetodermia and brachydactyly type E (Q46718) (← links)
- Syndromes with face or limb anomalies as a major feature (Q46719) (← links)
- Otomandibular dysplasia (Q46720) (← links)
- Syndromes with connective tissue involvement as a major feature (Q46721) (← links)
- Waardenburg-Shah syndrome (Q46722) (← links)
- MURCS association (Q46723) (← links)
- Syndromes with premature ageing appearance as a major feature (Q46724) (← links)
- Disorders of peroxisome biogenesis (Q46725) (← links)
- Marfan syndrome or Marfan-related disorders (Q46726) (← links)
- Syndromic genetic deafness (Q46727) (← links)
- Oral-facial-digital syndrome (Q46728) (← links)
- Yunis-Varon disease (Q46729) (← links)
- Fraser syndrome (Q46730) (← links)
- Neuropathy with hearing impairment (Q46731) (← links)
- Usher syndrome (Q46732) (← links)
- Cronkhite-Canada syndrome (Q46733) (← links)
- Acrofacial dysostoses (Q46734) (← links)
- Progressive deafness with stapes fixation (Q46735) (← links)
- Syndromes with obesity as a major feature (Q46736) (← links)
- Disorders of peroxisomal alpha-, beta- or omega-oxidation (Q46737) (← links)
- Syndromes with multiple structural anomalies, without predominant body system involvement (Q46738) (← links)
- Syndromes with multiple structural anomalies, not of environmental origin (Q46739) (← links)
- Oromandibular-limb anomaly syndrome (Q46740) (← links)
- Fronto-otopalatodigital syndromes (Q46741) (← links)
- Ectopic spleen (Q46742) (← links)
- Congenital asplenia (Q46743) (← links)
- Structural developmental anomalies of spleen (Q46744) (← links)
- Polysplenia (Q46745) (← links)
- Congenital adrenal hypoplasia (Q46746) (← links)
- Total mirror imagery (Q46747) (← links)
- Conjoined twins (Q46748) (← links)
- Left isomerism (Q46749) (← links)
- Right isomerism (Q46750) (← links)
- Complete trisomy 21 (Q46751) (← links)
- Maternal imprinting error (Q46753) (← links)
- Duplications of chromosome 22 (Q46755) (← links)
- Duplications of chromosome 12 (Q46757) (← links)
- Duplications of chromosome 2 (Q46759) (← links)
- Duplications of chromosome 16 (Q46761) (← links)
- Duplications of chromosome 19 (Q46763) (← links)
- Duplications of chromosome 5 (Q46765) (← links)
- Duplications of chromosome 10 (Q46767) (← links)
- Duplications of chromosome 13 (Q46769) (← links)
- Male with 46,XX karyotype (Q46771) (← links)
- Uniparental disomies of maternal origin (Q46773) (← links)
- Number anomalies of chromosome X (Q46775) (← links)
- Duplications of chromosome 6 (Q46777) (← links)
- Uniparental disomies of paternal origin (Q46779) (← links)
