ERF Results

ERF

ETS2 repressor factor
05/31/2017

ERFE

erythroferrone

SLC9A3R2

SLC9A3 regulator 2

FOXRED2

FAD dependent oxidoreductase domain containing 2

HBS1L

HBS1 like translational GTPase

MTERF1

mitochondrial transcription termination factor 1

MTERF2

mitochondrial transcription termination factor 2

MTERF3

mitochondrial transcription termination factor 3

MTERF4

mitochondrial transcription termination factor 4

PDZK1

PDZ domain containing 1

SERF1A

small EDRK-rich factor 1A

SERF1B

small EDRK-rich factor 1B

SERF2

small EDRK-rich factor 2

SLC9A3R1

SLC9A3 regulator 1

FABP9

fatty acid binding protein 9

TERF1

telomeric repeat binding factor 1

TERF2

telomeric repeat binding factor 2

TERF2IP

TERF2 interacting protein

TFAP2C

transcription factor AP-2 gamma

ELF2

E74 like ETS transcription factor 2

osteogenesis imperfecta type 7

MONDO_0012536 Condition
OI7
10/17/2018

osteogenesis imperfecta type 1

MONDO_0008146 Condition
Mild osteogenesis imperfecta
08/22/2019

dentinogenesis imperfecta (disease)

MONDO_0018849 Condition
dentinogenesis imperfecta
04/17/2018

osteogenesis imperfecta type 8

MONDO_0012581 Condition
OI8
05/31/2017

osteogenesis imperfecta type 9

MONDO_0009805 Condition
OI9
11/12/2018

amelogenesis imperfecta hypomaturation type 2A3

MONDO_0013181 Condition
AI2A3
10/17/2018

osteogenesis imperfecta type 5

MONDO_0012591 Condition
OI type 5

amelogenesis imperfecta hypomaturation type 2A2

MONDO_0012926 Condition
AI2A2

diphallus rachischisis imperforate anus

MONDO_0022990 Condition

microtia-eye coloboma-imperforation of the nasolacrimal duct syndrome

MONDO_0012739 Condition
Balikova-Vermeesch syndrome

intestinal perforation

MONDO_0006807 Condition
Perforation of intestine

Ehlers-Danlos/osteogenesis imperfecta syndrome

MONDO_0016470 Condition
EDS/OI syndrome

medulloadrenal hyperfunction

MONDO_0001473 Condition

amelogenesis imperfecta, type Ij; AI1J

MONDO_0015008 Condition
Amelogenesis Imperfecta, Type IJ

deafness, autosomal dominant 39, with dentinogenesis imperfecta 1

MONDO_0011571 Condition
Deafness, Autosomal Dominant 39, With Dentinogenesis Imperfecta type 1

epidermolysis bullosa simplex superficialis

MONDO_0011869 Condition
EBSS

genetic hyperferritinemia without iron overload

MONDO_0016788 Condition
Benign hyperferritinemia

perforated corneal ulcer

MONDO_0001038 Condition

imperforate anus

MONDO_0001046 Condition
Congenital or infantile occlusion of anus