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
Linear skin defects with multiple congenital anomalies 2 C3550921
aplasia cutis congenita, Reticulolinear, with microcephaly, Facial Dysmorphism, and Other congenital anomalies 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
COX7B microphthalmia with linear skin defects syndrome C3550921
microphthalmia with linear skin defects syndrome caused by mutation in COX7B C3550921
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