MedGen Find_IDs Find_Terms Annotation
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created at 2024-09-19 07:43:07 UTC
updated at 2024-09-23 18:19:38 UTC
MedGen CUI
Namespace: https://www.ncbi.nlm.nih.gov/medgen/
622,528 entries

There is 0 pattern entry.

Label
Id
APLCC C3550921
LSDMCA2 C3550921
aplasia cutis congenita, Reticulolinear, with microcephaly, Facial Dysmorphism, and Other congenital anomalies C3550921
APLASIA CUTIS CONGENITA, RETICULOLINEAR, WITH MICROCEPHALY, FACIAL DYSMORPHISM, AND OTHER CONGENITAL ANOMALIES C3550921
LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2 C3550921
COX7B microphthalmia with linear skin defects syndrome C3550921
Linear skin defects with multiple congenital anomalies 2 C3550921
linear skin defects with multiple congenital anomalies 2 C3550921
linear skin defects with multiple congenital anomalies 2, X-linked dominant C3550921
linear skin defects with multiple congenital anomalies type 2 C3550921
microphthalmia with linear skin defects syndrome caused by mutation in COX7B C3550921
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