syndromic disease hereditary disease camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye https://github.com/monarch-initiative/mondo/issues/6744 https://www.malacards.org/card/camptodactyly_myopia_and_fibrosis_of_the_medial_rectus_muscle_of_eye MESH:C535876 SCTID:715986009 A rare multiple congenital anomalies syndrome characterized by the association of camptodactyly, multiple eye defects (fibrosis of the medial rectus muscle, severe myopia, ptosis and exophthalmos), scoliosis, flexion contractures and facial anomalies (arched eyebrows, facial asymmetry with an abnormal skull shape, a prominent nose, small mouth, low-set and dysplastic ears, and a low nuchal hairline). Rozin hertz Goodman syndrome Orphanet:1323 camptodactyly, joint contractures, facial skeletal defects camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye MEDGEN:355918 UMLS:C1865133 GARD:0000216 OMIM:602612 MONDO:0011262 multiple congenital anomalies/dysmorphic syndrome without intellectual disability dysostosis