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hypogonadotropic hypogonadism 7 with or without anosmia
Summary
- Definition
- A hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the GNRHR gene on chromosome 4q13, sometimes in association with mutation in another gene. No patients with anosmia have been reported.
- Super Class
- autosomal recessive disease hypogonadotropic hypogonadism
External Links
- Disease Ontology
- DOID:0090078
- Mondo Disease Ontology
-
- MONDO:0005152
- MONDO:0007794
- MONDO:0007844
- MONDO:0009482
- MONDO:0010635
- MONDO:0012528
- MONDO:0012880
- MONDO:0012988
- MONDO:0013099
- MONDO:0013910
- MONDO:0013911
- MONDO:0013912
- MONDO:0013913
- MONDO:0013914
- MONDO:0013915
- MONDO:0013926
- MONDO:0013961
- MONDO:0014102
- MONDO:0014103
- MONDO:0014105
- MONDO:0014106
- MONDO:0014107
- MONDO:0014461
- MONDO:0015127
- MONDO:0015770
- MONDO:0015789
- MONDO:0016384
- MONDO:0016553
- MONDO:0018555
- MONDO:0018762
- MONDO:0018800
- MONDO:0019032
- MONDO:0019614
- MONDO:0019617
- MONDO:0019618
- MONDO:0019824
- MONDO:0019832
- MONDO:0019841
- OMIM
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 128 | ADH5 | alcohol dehydrogenase 5 (class III), chi polypeptide | |
| 176 | ACAN | aggrecan | |
| 412 | STS | steroid sulfatase | |
| 960 | CD44 | CD44 molecule (IN blood group) | |
| 1586 | CYP17A1 | cytochrome P450 family 17 subfamily A member 1 | |
| 1588 | CYP19A1 | cytochrome P450 family 19 subfamily A member 1 | |
| 1604 | CD55 | CD55 molecule (Cromer blood group) | |
| 1650 | DDOST | dolichyl-diphosphooligosaccharide--protein glycosyltransferase non-catalytic subunit | |
| 1890 | TYMP | thymidine phosphorylase | |
| 2131 | EXT1 | exostosin glycosyltransferase 1 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q8IY17 | Patatin-like phospholipase domain-containing protein 6 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000786 | Primary amenorrhea |
| HP:0008527 | Congenital sensorineural hearing impairment |
| HP:0000118 | Phenotypic abnormality |
| HP:0002750 | Delayed skeletal maturation |
| HP:0000027 | Azoospermia |
| HP:0005280 | Depressed nasal bridge |
| HP:0000316 | Hypertelorism |
| HP:0012385 | Camptodactyly |
| HP:0000938 | Osteopenia |
| HP:0000013 | Hypoplasia of the uterus |
