All terms in CLO
| Label | Id | Description |
|---|---|---|
| HEV0496 cell | CLO_0051329 | [Register: Imai, Takashi] |
| GM17729 cell | CLO_0016991 | [ XXY SYNDROME; KLINEFELTER SYNDROME ANEUPLOID CHROMOSOME NUMBER - NON-TRISOMIC] |
| HEV0492 cell | CLO_0051328 | [Register: Imai, Takashi] |
| GM17723 cell | CLO_0016990 | [ SOLUTE CARRIER FAMILY 17, MEMBER 5; SLC17A5 SALLA DISEASE] |
| sialuria | DOID_3659 | |
| HEV0482 cell | CLO_0051327 | [Register: Imai, Takashi] |
| GM17237 cell | CLO_0014330 | [ HUMAN VARIATION PANEL - CAUCASIAN PANEL OF 200 HUMAN VARIATION PANEL - CAUCASIAN PANEL OF 100 (SET 1) HUMAN VARIATION PANEL - CAUCASIAN PANEL OF 50] |
| GM17731 cell | CLO_0016993 | [ FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1A; FSHMD1A (FSHD) FSHD GENE 1; FRG1] |
| immortal human rhomboid-derived myoblast cell line cell | CLO_0000828 | |
| facioscapulohumeral muscular dystrophy | EFO_0000491 | [An autosomal dominant degenerative muscle disease characterized by slowly progressive weakness of the muscles of the face, upper-arm, and shoulder girdle. The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation. This tends to be followed by facial weakness, primarily involving the orbicularis oris and orbicularis oculi muscles. (Neuromuscul Disord 1997;7(1):55-62; Adams et al., Principles of Neurology, 6th ed, p1420)] |
| HEV0463 cell | CLO_0051326 | [Register: Imai, Takashi] |
| GM17726 cell | CLO_0016992 | [ FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; TYPE UNKNOWN (FSHD)] |
| ND02532 cell | CLO_0014331 | [ CONTROL PANEL FOR YOUNG ONSET PARKINSON'S; UNAFFECTED INDIVIDUALS POPULATION/CONVENIENCE CONTROL] |
| HEV0455 cell | CLO_0051325 | [Register: Imai, Takashi] |
| GM17733 cell | CLO_0016995 | [ HUMAN VARIATION PANEL - HAN PEOPLE OF LOS ANGELES PANEL OF 24 HUMAN VARIATION PANEL - HAN PEOPLE OF LOS ANGELES PANEL OF 100 HUMAN VARIATION PANEL - HAN PEOPLE OF LOS ANGELES PANEL OF 16] |
| GM17238 cell | CLO_0014332 | [ HUMAN VARIATION PANEL - CAUCASIAN PANEL OF 200 HUMAN VARIATION PANEL - CAUCASIAN PANEL OF 50 HUMAN VARIATION PANEL - CAUCASIAN PANEL OF 100 (SET 1)] |
| HEV0448 cell | CLO_0051324 | [Register: Imai, Takashi] |
| DA05346 cell | CLO_0014333 | [ DIABETES MELLITUS FAMILY SAMPLE] |
| GM17730 cell | CLO_0016994 | [ AUTISTIC DISORDER TRANSLOCATED CHROMOSOME] |
| autistic disorder | DOID_12849 |