Albright's hereditary osteodystrophy
(Q4712685)
osteochondrodysplasia that has material basis in lack of responsiveness to parathyroid hormone which results in shortening and widening of long bones of the located in hand or located in foot along with short stature, obesity, and rounded face
osteochondrodysplasia that has material basis in lack of responsiveness to parathyroid hormone which results in shortening and widening of long bones of the located in hand or located in foot along with short stature, obesity, and rounded face
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Current Data About
Albright's hereditary osteodystrophy
(P31) |
(Q929833)
(Q112193867) |
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(P279) |
(Q819207)
(Q55788263) |
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(P1343) |
(Q19558994)
|
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(P1692) |
275.49
|
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(P1748) |
C118434
C129721
|
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(P1995) |
(Q162606)
|
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(P2293) |
(Q14905160)
|
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(P2888) |
http://purl.obolibrary.org/obo/DOID_0080053
http://identifiers.org/doid/DOID:0080053
http://www.orpha.net/ORDO/Orphanet_665 http://www.orpha.net/ORDO/Orphanet_79443 |
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(P5008) |
(Q4099686)
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other details
aliases |
Albright hereditary osteodystrophy pseudohypoparathyroidism type 1a PSEUDOHYPOPARATHYROIDISM, TYPE IA Php 1A PHP1A Albright hereditary osteodystrophy-PHP syndrome Ia PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A AHO-PHP syndrome Ia Albright Hereditary Osteodystrophy With Multiple Hormone Resistance pseudohypoparathyroidism Ia pseudohypoparathyroidism 1a |
description | osteochondrodysplasia that has material basis in lack of responsiveness to parathyroid hormone which results in shortening and widening of long bones of the located in hand or located in foot along with short stature, obesity, and rounded face |
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