TMEM94-associated congenital heart defect-facial dysmorphism-developmental delay syndrome

Orpha code: 562569OMIM code: 618316

Definition

A rare, genetic, neurodevelopmental disorder characterized by global developmental delay, congenital heart defects, generalized hypertrichosis and dysmorphic facial features, most commonly triangular face, thick arched eyebrows, widely spaced eyes, posteriorly rotated low set ears, depressed nasal bridge, broad nasal root and tip, and pointed chin.

Disease data
Classification

Malformation syndrome

ORPHA code
562569
OMIM code
618316
ICD10 code
Q87.8
ICD11 code
-

No additional description.

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