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searching for Microdontia 7 found (189 total)

Michel aplasia (611 words) [view diff] exact match in snippet view article find links to article

is associated with LAMM syndrome (labyrinthine aplasia, microtia and microdontia), which is caused by mutation FGF3 gene on chromosome 11q13 which encodes

FGF3 (790 words) [view diff] exact match in snippet view article find links to article

syndromic deafness characterized by inner ear agenesis, microtia, and microdontia". Am. J. Hum. Genet. 80 (2): 338–44. doi:10.1086/510920. PMC 1785350

Betula pubescens (2,080 words) [view diff] exact match in snippet view article find links to article

Schrad. ex Regel Betula major Gilib. Betula megaloptera Kindb. Betula microdontia Kindb. Betula murithii Gaudin ex Regel Betula nigricans Wender. Betula

List of diseases (S) (1,933 words) [view diff] exact match in snippet view article

with multiple anomalies of hands and feet Symphalangism, distal, with microdontia, dental pulp stones, and narrowed zygomatic arch Syncamptodactyly scoliosis

List of diseases (M) (2,469 words) [view diff] exact match in snippet view article

correctopia macular hypoplasia Microcornea glaucoma absent frontal sinuses Microdontia hypodontia short stature Microencephaly Microgastria limb reduction defect

Sensorineural hearing loss (9,622 words) [view diff] exact match in snippet view article find links to article

syndromes such as LAMM syndrome (labyrinthine aplasia, microtia and microdontia), Pendred syndrome, branchio-oto-renal syndrome, CHARGE syndrome GATA2

List of OMIM disorder codes (18,877 words) [view diff] exact match in snippet view article find links to article

611022; RDX Deafness, congenital with inner ear agenesis, microtia, and microdontia; 610706; FGF3 Deafness, digenic GJB2/GJB6; 220290; GJB6 Deafness, digenic