Microcephaly, microphthalmia, ectrodactyly of lower limbs, prognathism syndrome (Q94964): Difference between revisions

From determinar.ia.br - Determine suas informações
‎Created a new Item
 
‎Changed label, description and/or aliases in pt-br, en
description / pt-brdescription / pt-br
 
Síndrome MMEP é uma forma sindrômica congênita de malformação mão/pé fendidos (SHFM), e é caracterizada por microcefalia, microftalmia, ectrodactilia de membros inferiores e prognatismo.
description / endescription / en
 
The MMEP syndrome is a congenital syndromic form of split-hand/foot malformation (SHFM), and is characterised by microcephaly, microphthalmia, ectrodactyly of the lower limbs and prognathism.

Revision as of 10:32, 16 August 2026

The MMEP syndrome is a congenital syndromic form of split-hand/foot malformation (SHFM), and is characterised by microcephaly, microphthalmia, ectrodactyly of the lower limbs and prognathism.
Language Label Description Also known as
default for all languages
ID_245558058
    English
    Microcephaly, microphthalmia, ectrodactyly of lower limbs, prognathism syndrome
    The MMEP syndrome is a congenital syndromic form of split-hand/foot malformation (SHFM), and is characterised by microcephaly, microphthalmia, ectrodactyly of the lower limbs and prognathism.

      Statements