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Diseases
Genes (1023)
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ZEB2
Microphthalmia
Hypertelorism
Mowat–wilson Syndrome
PMM2
Pmm2 Deficiency
Hypertelorism
ASL
Argininosuccinic Aciduria
TTPA
Familial Isolated Vitamin E Deficiency
FOXP2
Foxp2-Related Speech And Language Disorder
PQBP1
Microphthalmia
Renpenning's Syndrome
ADGRG1
Bilateral Frontoparietal Polymicrogyria
FOXG1
Foxg1 Syndrome
TBX19
Acth Deficiency, Isolated
TAF1
Mental Retardation, X-Linked, Syndromic 33
IFIH1
Singleton Merten Syndrome
MSTN
Myostatin-Related Muscle Hypertrophy
PRSS56
Microphthalmia
COX4I2
Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, And Calvarial Hyperostosis
RB1
Pinealoblastoma
Microphthalmia
Hypertelorism
Trilateral Retinoblastoma
TBR1
Microphthalmia
Hypertelorism
Intellectual Developmental Disorder With Autism And Speech Delay
ASS1
Argininosuccinic Aciduria
Citrullinemia Type I
FH
Vocal Cord Paralysis
Microphthalmia
Hypertelorism
Fumarase Deficiency
MFRP
Microphthalmia
PITX3
Microphthalmia