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Results 1 - 10 of 125 for Tooth agenesis
  1. MSX1 gene 
    ... 1 MSX1_HUMAN OFC5 Tests of MSX1 PubMed TOOTH AGENESIS, SELECTIVE, 1; STHAG1 MSH HOMEOBOX 1; MSX1 WITKOP ... C. Haploinsufficiency of MSX1: a mechanism for selective tooth agenesis. Mol Cell Biol. 1998 Oct;18(10):6044- ...
    https://medlineplus.gov/genetics/gene/msx1 - Genetics
  2. WNT10A gene 
    ... also frequently associated with a condition called nonsyndromic tooth agenesis. This condition causes one or more teeth not ... ectodermal dysplasias, "nonsyndromic" suggests that in these cases tooth agenesis occurs without the other signs and symptoms of ...
    https://medlineplus.gov/genetics/gene/wnt10a - Genetics
  3. EDAR gene 
    ... in some people with a condition called nonsyndromic tooth agenesis. This condition causes one or more teeth not ... ectodermal dysplasias, "nonsyndromic" suggests that in these cases tooth agenesis occurs without the other signs and symptoms of ...
    https://medlineplus.gov/genetics/gene/edar - Genetics
  4. EDA gene 
    ... in some people with a condition called nonsyndromic tooth agenesis. This condition causes one or more teeth not ... ectodermal dysplasias, "nonsyndromic" suggests that in these cases tooth agenesis occurs without the other signs and symptoms of ...
    https://medlineplus.gov/genetics/gene/eda - Genetics
  5. Keratoderma with woolly hair 
    ... Registry: Cardiomyopathy, dilated, with wooly hair, keratoderma, and tooth agenesis Genetic Testing Registry: Wooly hair-palmoplantar keratoderma syndrome ...
    https://medlineplus.gov/.../condition/keratoderma-with-woolly-hair - Genetics
  6. Oculodentodigital dysplasia 
    ... to vision loss. Affected individuals also frequently have tooth abnormalities, such as small or missing teeth, weak enamel, multiple cavities, and early tooth loss. Other common features of this condition include ...
    https://medlineplus.gov/.../condition/oculodentodigital-dysplasia - Genetics
  7. Laryngo-onycho-cutaneous syndrome 
    ... its other functions leads to the nail and tooth abnormalities that occur in this condition. LAMA3 This condition ...
    https://medlineplus.gov/.../laryngo-onycho-cutaneous-syndrome - Genetics
  8. PITX2 gene 
    ... protein can also lead to distinctive facial features, tooth abnormalities, and problems with development of other parts of ...
    https://medlineplus.gov/genetics/gene/pitx2 - Genetics
  9. LAMA3 gene 
    ... its other functions leads to the nail and tooth abnormalities that occur in this condition.LOC syndrome is ...
    https://medlineplus.gov/genetics/gene/lama3 - Genetics
  10. DSP gene 
    ... EBLA CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS; DCWHKTA KERATOSIS PALMOPLANTARIS STRIATA II; PPKS2 NCBI Gene ...
    https://medlineplus.gov/genetics/gene/dsp - Genetics
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