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Category:Genetic disorders with OMIM but no gene

From WikiMD's Medical Encyclopedia

Pages in category "Genetic disorders with OMIM but no gene"

The following 26 pages are in this category, out of 26 total.

A

  • Abruzzo–Erickson syndrome
  • Accessory auricle
  • Acrogeria, Gottron type
  • Aicardi syndrome
  • Aplasia cutis congenita

B

  • Blue diaper syndrome
  • Brugada syndrome

C

  • Catel–Manzke syndrome

D

  • DOOR syndrome

F

  • Primary Familial Brain Calcification
  • Fibrochondrogenesis

G

  • Gastroschisis
  • GLB1

H

  • Hydrocephalus-cleft palate-joint contractures syndrome

L

  • LAMA2 related congenital muscular dystrophy
  • LMNA-related congenital muscular dystrophy

M

  • Maffucci syndrome
  • Mandibulofacial dysostosis-microcephaly syndrome

N

  • Neonatal hemochromatosis

O

  • Oculopharyngodistal myopathy

P

  • Photic sneeze reflex
  • Proteus syndrome

S

  • SMN1

W

  • Wallis–Zieff–Goldblatt syndrome

Y

  • Yunis–Varon syndrome

Z

  • Zori–Stalker–Williams syndrome
Retrieved from "https://wikimd.org/index.php?title=Category:Genetic_disorders_with_OMIM_but_no_gene&oldid=6172810"
Category:
  • Genetic diseases and disorders
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  • This page was last edited on 22 January 2025, at 07:59.
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