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ENLinear Skin Defects with Multiple Congenital Anomalies 1 (LSDMCA1)
Alias:
Midas Syndrome
Mls Syndrome
Mcops7
Microphthalmia, Syndromic 7
Microphthalmia with Linear Skin Defects Syndrome
Microphthalmia-Dermal Aplasia-Sclerocornea Syndrome
Syndromic Microphthalmia Type 7
Microphthalmia, Dermal Aplasia, and Sclerocornea
Microphthalmia with Linear Skin Defects
Lsdmca1
Mls
Microphthalmia, Dermal Aplasia, Sclerocornea Syndrome
Linear Skin Defects with Multiple Congenital Anomalies
Microphthalmia with Linear Skin Lesions Syndrome
Microphthalmia with Linear Skin Defect Syndrome
Microphthalmia, Dermal Aplasia and Sclerocornea
Microphthalmia, Syndromic, 7
Syndromic Microphthalmia 7
Microphthalmia Syndromic 7
Syndromic Microphthalmia-7
Midas
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Linear Skin Defects with Multiple Congenital Anomalies 1, also known as midas syndrome, is related to linear skin defects with multiple congenital anomalies 2 and microphthalmia. An important gene associated with Linear Skin Defects with Multiple Congenital Anomalies 1 is HCCS (Holocytochrome C Synthase), and among its related pathways/superpathways is Peroxisomal lipid metabolism. The drugs Zolmitriptan and Neurotransmitter Agents have been mentioned in the context of this disorder. Affiliated tissues include skin and eye, and related phenotypes are corneal opacity and aplasia/hypoplasia of the skin
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MALACARDS
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