loading...| Preferred Name | Leydig Cell Hypoplasia | |
| Synonyms |
Leydig Cell Hypoplasia with Male Pseudohermaphroditism Leydig Cell Hypoplasia, Complete Leydig Cell Agenesis LH Resistance Due To LH Receptor Deactivation Leydig Cell Hypoplasia, Type II Hypergonadotropic Hypogonadism, Male, Due To LHCGR Defect Leydig Cell Hypoplasia, Partial Leydig Cell Hypoplasia, Type I Male Hypergonadotropic Hypogonadism Due To LHCGR Defect 46,XY Disorder of Sex Development Due To LH Defects Luteinizing Hormone Resistance, Female |
|
| ID |
http://purl.bioontology.org/ontology/MESH/C562567 |
|
| altLabel |
Leydig Cell Hypoplasia with Male Pseudohermaphroditism Leydig Cell Hypoplasia, Complete Leydig Cell Agenesis LH Resistance Due To LH Receptor Deactivation Leydig Cell Hypoplasia, Type II Hypergonadotropic Hypogonadism, Male, Due To LHCGR Defect Leydig Cell Hypoplasia, Partial Leydig Cell Hypoplasia, Type I Male Hypergonadotropic Hypogonadism Due To LHCGR Defect 46,XY Disorder of Sex Development Due To LH Defects Luteinizing Hormone Resistance, Female |
|
| cui |
C3714042 C2673497 C0860158 C0266432 C3668935 |
|
| Has mapping qualifier | ||
| HM |
D058490 D013737/Q000002 |
|
| Inverse of RB |
0 |
|
| Mapped to | ||
| MDA |
20121105 |
|
| MeSH Frequency |
21 |
|
| MMR |
20131024 |
|
| notation |
C562567 |
|
| prefLabel |
Leydig Cell Hypoplasia |
|
| SC |
3 |
|
| Scope Statement |
mutation in LHCGR |
|
| TERMUI |
T800955 T809787 T845955 T831203 T809785 T800952 T841918 T800954 T845953 T845954 T831202 T827123 |
|
| TH |
OMIM (2013) GHR (2014) |
|
| tui |
T047 T019 |