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Deep Research Advanced Download Gene List
  • KRT17
    • Teeth Present At Birth
    • Steatocystoma Multiplex
    • Pachyonychia Congenita 2
  • SPECC1L
    • Teeth Present At Birth
    • Hypertelorism, Teebi Type
  • POC1A
    • Short Stature-Onychodysplasia-Facial Dysmorphism-Hypotrichosis Syndrome
  • RNU4ATAC
    • Roifman Syndrome
  • AMPD2
    • Pontocerebellar Hypoplasia Type 9
  • GLUL
    • Congenital Brain Dysgenesis Due To Glutamine Synthetase Deficiency
  • NSDHL
    • Ck Syndrome
  • IARS1
    • Growth Delay-Intellectual Disability-Hepatopathy Syndrome
  • DIAPH1
    • Progressive Microcephaly-Seizures-Cortical Blindness-Developmental Delay Syndrome
  • MYCN
    • Pinealoblastoma
    • Feingold Syndrome Type 1
  • KRT16
    • Pachyonychia Congenita 2
  • MIR17HG
    • Feingold Syndrome Type 1
  • GJA1
    • Hallermann-Streiff Syndrome
  • KRT6B
    • Steatocystoma Multiplex
    • Pachyonychia Congenita 2
  • FLNA
    • Teeth Present At Birth
    • Intestinal Pseudoobstruction With Patent Ductus Arteriosus And Natal Teeth
  • KRT6A
    • Pachyonychia Congenita 2
  • SART3
    • Disseminated Superficial Actinic Porokeratosis
  • KRT10
    • Pachyonychia Congenita 2
  • MARK3
    • Visual Impairment And Progressive Phthisis Bulbi
  • TRAF6
    • Ectodermal Dysplasia 12, Hypohidrotic/hair/tooth/nail Type

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