U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Search results

Items: 2

1.

Holoprosencephaly 3

Any holoprosencephaly in which the cause of the disease is a mutation in the SHH gene. [from MONDO]

MedGen UID:
327125
Concept ID:
C1840529
Disease or Syndrome
2.

Abnormality of the nose

An abnormality of the nose. [from HPO]

MedGen UID:
539457
Concept ID:
C0265736
Congenital Abnormality

Supplemental Content

Find related data

Search details

See more...

Recent activity