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| created at |
2021-12-22 03:08:20 UTC |
| updated at |
2021-12-22 07:06:09 UTC |
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MONDO_bioport_pref_name
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183,974 entries
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There is 0 pattern entry.
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CGHT
|
7610 |
|
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EBS
|
17610 |
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EEB
|
17610 |
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HTC3
|
7610 |
|
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chromosome 17Q24.2-q24.3 deletion syndrome
|
7610 |
|
|
chromosome 17Q24.2-q24.3 Duplication syndrome
|
7610 |
|
|
gingival fibromatosis-hypertrichosis syndrome
|
7610 |
|
|
epidermolysis bullosa intraepidermic
|
17610 |
|
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scoliosis, and retinitis pigmentosa rhizomelic dysplasia
|
C537610 |
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hereditary gingival fibromatosis with hypertrichosis
|
7610 |
|
|
hirsutism-congenital gingival hyperplasia syndrome
|
7610 |
|
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congenital generalized hypertrichosis terminalis
|
7610 |
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hypertrichosis with or without gingival hyperplasia
|
7610 |
|
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hypertrichosis terminalis, generalized, with gingival hyperplasia
|
7610 |
|
|
hypertrichosis terminalis, generalized, with or without gingival hyperplasia
|
7610 |
|
