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Diseases
Genes (176)
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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