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Items: 2

1.

Neu-Laxova syndrome 1

Any Neu-Laxova syndrome in which the cause of the disease is a mutation in the PHGDH gene. [from MONDO]

MedGen UID:
1633287
Concept ID:
C4551478
Disease or Syndrome
2.

Yellow subcutaneous tissue covered by thin, scaly skin

MedGen UID:
340563
Concept ID:
C1850533
Finding

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